ライフサイエンスコーパス: long arm

1 ned within the pericentromeric region of the long arm.

2 ation frequency than the largely euchromatic long arm.

3 region and the remaining 24 loci were on the long arm.

4 tion to homozygosity along the length of the long arm.

5 RBMY genes in interval 6 of the Y chromosome long arm.

6 ins on the short arm and 1 of 15 bins on the long arm.

7 c maternal isodisomy and heterodisomy of the long arm.

8 n approximately 32-cM terminal region of the long arm.

9 omosomes exhibit a single site on the distal long arm.

10 clustered in two breakpoint hotspots on the long arm.

11 ed from mice lacking the entire Y chromosome long arm.

12 positive interference was restricted to the long arms.

13 ng 25 polymorphic loci on both the short and long arms.

14 olecules with one short arm and two flexible long arms.

15 s due to an inherent curvature in one of the long arms.

16 ntical functional domains at the ends of the long arms.

17 morphic markers mapped to both the short and long arms.

18 regions of short arms and middle regions of long arms.

19 lymorphic markers covering almost the entire long arm; 46 loci, consisting of mutually recombining ma

20 egions of deletion ranging across the entire long arm (6q), with no defined recurrent breakpoint yet

21 from the DAZ locus of the human Y chromosome long arm, a locus in which the entire DAZ gene as well a

22 to the pericentromeric region of the group-5 long arm anchored to the rice BACs located in the recent

23 ntire plakin domain has an "L" shape, with a long arm and a short arm held at a perpendicular angle.

24 accounts for 4% of the physical size of the long arm and at least 30% of the recombination along the

25 Most of these are small-bodied taxa with long arms and broad wings comprised of vaned feathers, b

26 vely gene-poor regions on both the short and long arms and having good synteny with rice were discove

27 cturally altered chromosomes with consistent long arms and variable short arms, as well as the presen

28 mely disassembly of the SC proteins from the long arms, and is dependent on the crossover (CO) promot

29 mosomal arms recombined at higher rates than long arms, and recombination was more frequent in telome

30 and demonstrated linkage to a region on the long arm between DXS548 and Xqter.

31 integrin alpha6 beta1 and at least one other long arm-binding beta1 integrin.

32 s a complex epithelial tube that consists of long arms composed predominantly of germline tissue as w

33 thyleneoxy) arm para to the ester linkages, "long-armed" cryptand 4, possessed diminished binding wit

34 of a whole chromosome 5 or a deletion of the long arm, del(5q), is a recurring abnormality in maligna

35 of a whole chromosome 5 or a deletion of the long arm, del(5q), is a recurring abnormality in myelody

36 of a whole chromosome 7 or a deletion of the long arm, del(7q), are recurring abnormalities in malign

37 n rates, whereas functional chromosomes with long-arm deletions had low (approximately 85%) transmiss

38 chromosome, located at the distal end of the long arm euchromatic region, is required for normal sper

39 binding site has been known to reside in the long arm globular domain (G domain).

40 me with a small segment translocation on the long arm in the MF progenies (2n = 34).

41 The long arm is 24.0 nm long and accommodates four stably fo

42 influences the placement of chiasmata in the long arm, it is most likely that the translocation forma

43 to short arm loci in four tumors and to the long arm loci in 12 tumors, suggesting the presence of t

44 More than 60% of the long arm markers were present in three major clusters th

45 Deletions on the mouse Y-chromosome long arm (MSYq) lead to teratozoospermia and in severe c

46 The B chromosome long arm must be present in the same nucleus for the cen

47 dem arrangement attached to a segment of the long arm of a supernumerary B chromosome.

48 erminal domain of chromatin that extends the long arm of Ab10 to approximately 1.3 times the size of

49 lies has provided evidence of linkage to the long arm of chromosome 1 (1q24-25).

50 localized to a 0.5-centiMorgan region on the long arm of chromosome 1 at q31.3.

51 performed high-density mapping of the entire long arm of chromosome 1 in 13 CDC tumor samples.

52 utations to a 2-cM overlapping region of the long arm of chromosome 1 of tomato, a region not previou

53 lications involving all or part of the whole long arm of chromosome 1 presumably occur as secondary a

54 Relative overexpression of genes on the long arm of chromosome 1 was shown in all tumours that s

55 like factor CTD6, which is located at on the long arm of chromosome 1, area 36.2-36.1 in the region o

56 arkers from 81.8-242.9 cM are located in the long arm of chromosome 1.

57 nt to the pericentric heterochromatin on the long arm of chromosome 1.

58 n other regions of the genome, including the long arm of Chromosome 1.

59 b family (19 affected relatives) maps to the long arm of chromosome 10 (10q25; nonparametric linkage

60 The l2 locus was mapped to the long arm of chromosome 10 and positional cloning reveale

61 persyn genomic locus and localized it to the long arm of chromosome 10 in the q23.2-q23.3 region.

62 togenetic studies indicated that loss of the long arm of chromosome 10 is a frequent event in small c

63 The long arm of chromosome 10 is frequently affected by alle

64 sceptibility gene for type 2 diabetes to the long arm of chromosome 10, where we have previously iden

65 rt arm of chromosome 2, and snm2 maps to the long arm of chromosome 10.

66 sor gene that resides at region 24-26 of the long arm of chromosome 10.

67 0 tumors had at least one allele loss on the long arm of chromosome 10.

68 an approximately 52 kb of the genome, on the long arm of chromosome 10.

69 Deletions of the long arm of chromosome 11 (11q) have been noted in prima

70 Abnormalities of the long arm of chromosome 11 are also evident in a wide var

71 Mutations in the ATM gene located on the long arm of chromosome 11 at 11q22-23 cause ataxia-telan

72 ommon adult leukemia, carry deletions of the long arm of chromosome 11 at 11q22-23.

73 mmediately adjacent to the centromere on the long arm of chromosome 11 in band 11q11.

74 uggest the tumor suppressor gene maps to the long arm of chromosome 11 in the region of 11q13-qter.

75 er(11)t(X;11) chromosome lacking most of the long arm of chromosome 11 into A388.6TG.c2 does not affe

76 f a melanoma tumor suppressor gene(s) on the long arm of chromosome 11 through suppression of tumorig

77 kage, a 40-Mb YAC contig covering the distal long arm of chromosome 11 was assembled.

78 ies tend to cluster in the lower half of the long arm of chromosome 11, indicating the possible prese

79 equently by terminal deletion of part of the long arm of chromosome 11, with breakpoints in 11q23.3-1

80 ave localized a tumor suppressor gene to the long arm of chromosome 11.

81 Both patients had abnormalities of the long arm of chromosome 11.

82 have been mapped to two distinct loci on the long arm of chromosome 11.

83 t a melanoma tumor suppressor resides on the long arm of chromosome 11.

84 isorder caused by a terminal deletion of the long arm of chromosome 11.

85 in families linking to the EVR1 locus on the long arm of chromosome 11.

86 es, the human MYCN gene was localized to the long arm of chromosome 12 band 12q24 which is the corres

87 hiwi maps to the long arm of chromosome 12, band 12q24.33, a genomic regi

88 hSPRY2 maps to the long arm of chromosome 13 (13q31.1), where loss of heter

89 Loss of heterozygosity (LOH) involving the long arm of chromosome 13 has been reported to occur in

90 nt of a tumor suppressor gene located on the long arm of chromosome 13, between the retinoblastoma (R

91 of patients with hemizygous deletions of the long arm of chromosome 13, we have defined a discrete re

92 epresentation toward locations on the distal long arm of chromosome 13, with no localizations noted i

93 ing a panel of 11 probes spanning the entire long arm of chromosome 13.

94 specimens analysed had an allele loss on the long arm of chromosome 13.

95 a single copy gene located in band 22 of the long arm of chromosome 14 (14q22).

96 he malignant and atypical tumors were on the long arm of chromosome 14.

97 l pyoderma gangrenosum-acne-arthritis to the long arm of chromosome 15 (maximum two-point LOD score,

98 The causative gene maps to the long arm of chromosome 15 but has not yet been identifie

99 include the imprinted region on the proximal long arm of chromosome 15 underlie a complex neurobehavi

100 ck a paternally derived copy of the proximal long arm of chromosome 15, and eat uncontrollably; in An

101 ataract was mapped to a 6.5-Mb region of the long arm of chromosome 15, at 22.33-24.2 between CYP11A

102 tected significant linkage to markers on the long arm of chromosome 15, in a region encompassing RLBP

103 c microsatellite markers spanning the entire long arm of chromosome 15.

104 AC) clone containing HuAZ2 at band 22 of the long arm of chromosome 15.

105 identified a second PKC locus (EKD2) on the long arm of chromosome 16 in a large Indian family with

106 The long arm of chromosome 16 is frequently deleted in human

107 total of 906 overgos were selected from the long arm of chromosome 16.

108 d together with a substantial portion of the long arm of chromosome 16.

109 cogene are located in close proximity on the long arm of chromosome 17 (17q11-21).

110 tary neuralgic amyotrophy gene to the distal long arm of chromosome 17 (17q24-qter).

111 with polymorphic short tandem repeats on the long arm of chromosome 17 revealed maximal pairwise LOD

112 ross a minimal 50-Mb region of primarily the long arm of chromosome 17 showed LOH in 8 cases, whereas

113 , while a third tribrid had a portion of the long arm of chromosome 17 translocated to mouse as its o

114 study to 70 tumors with 17 markers from the long arm of chromosome 17.

115 tosomal retinitis pigmentosa, located on the long arm of chromosome 17.

116 gest that allelic loss of sequences from the long arm of chromosome 18 may be a useful prognostic ind

117 netically to have a terminal deletion of the long arm of chromosome 18.

118 nal STRs spanning approximately 11 cM on the long arm of chromosome 18.

119 oss of the short arm of chromosome 1 and the long arm of chromosome 19, or 1p19q codeletion; and (c)

120 ization of scsae and 8 linked markers on the long arm of chromosome 1D.

121 Forty-two of the Rf alleles mapped to the long arm of chromosome 2 (2L), and 5 of these were furth

122 and high-resolution deletion mapping of the long arm of chromosome 2 (2q) in invasive cervical carci

123 ocus designation PDE6D) was localized to the long arm of chromosome 2 (2q35-q36) by fluorescence in s

124 ta) has been characterized and mapped to the long arm of chromosome 2 (HSA2q35-q36) where a new autos

125 pped a gene for ADHED (EDA3) to the proximal long arm of chromosome 2 (q11-q13).

126 One of these is on the long arm of chromosome 2 and is linked with loci encodin

127 cus has recently been assigned to the distal long arm of chromosome 2 in two families.

128 One locus on the long arm of chromosome 2 is coincident with genes encodi

129 ng approximately 40 centiMorgans (cM) on the long arm of chromosome 2.

130 opy number of DNA sequences derived from the long arm of chromosome 20 (20q) has been commonly observ

131 The l3mbtl1 gene is located on the long arm of chromosome 20 (q12), within a region commonl

132 eloproliferative neoplasms (MPN) affects the long arm of chromosome 20 and has been predicted to harb

133 lin-resistant type 2 diabetes located on the long arm of chromosome 20 around marker D20S196.

134 gene (or genes) in the "MODY1 region" of the long arm of chromosome 20 contributes to the development

135 -1 family, was cloned during a search on the long arm of chromosome 20 for genes whose expression and

136 Deletions of the long arm of chromosome 20 have been reported in a wide r

137 An acquired deletion of the long arm of chromosome 20 is a recurrent abnormality in

138 Deletion of the long arm of chromosome 20 represents the most common chr

139 splastic syndromes in whom a deletion of the long arm of chromosome 20 was detectable by G-banding an

140 A deletion of the long arm of chromosome 20, del(20q), is a recurring abno

141 ic loss at 39 highly polymorphic loci on the long arm of chromosome 20.

142 linkage was found for a 10-cM region on the long arm of chromosome 20q13.1-q13.2 between markers D20

143 In contrast to the distal half of the long arm of chromosome 21, the proximal half of approxim

144 Genes on the long arm of chromosome 22 and near the neurofibromatosis

145 ualized as MLH1 foci, localize to the distal long arm of chromosome 22 in 75% of human spermatocytes

146 egregation patterns linked to an area on the long arm of chromosome 22, localizing the gene encoding

147 this processed pseudogene to band 28 on the long arm of chromosome 3 by fluorescence in situ hybridi

148 sed to map the Def-1 gene to a region on the long arm of chromosome 3 that is genetically separable f

149 3/p73L) and localized the gene to the distal long arm of chromosome 3.

150 s frequently reveal additional copies of the long arm of chromosome 3.

151 as been placed on the tomato RFLP map on the long arm of chromosome 4 and does not demonstrate linkag

152 Deletions of the long arm of chromosome 4 detectable by cytogenetic analy

153 Loss of the long arm of chromosome 4 has been identified previously

154 P thus provides an additional marker for the long arm of chromosome 4 that should facilitate studies

155 The long arm of Chromosome 4 underwent a dramatic developmen

156 and mapped to the subtelomeric region of the long arm of chromosome 4(4H).

157 ne encoding human enamelin is located on the long arm of chromosome 4, in a region previously linked

158 nger domain containing genes, located on the long arm of chromosome 4, is expressed in a sharp peak d

159 ls contained an interstitial deletion in the long arm of chromosome 4, where the p16(INK4a) gene resi

160 sociated with a chromosomal inversion on the long arm of chromosome 4.

161 s encoded by a single gene at a locus on the long arm of chromosome 4.

162 hort arm of chromosomes 7A and 7D and on the long arm of chromosome 4A.

163 ed to deletion bins in the distal 42% of the long arm of chromosome 4B (4BL) were ordered in silico b

164 A heterozygous deletions of the long arm of chromosome 5 [del(5q)], observed in 40% of p

165 A deletion of the long arm of chromosome 5 is a recurring abnormality in m

166 Complete loss or deletion of the long arm of chromosome 5 is frequent in myelodysplastic

167 The distal portion of the long arm of chromosome 5 is linked to hypertension and c

168 alysis in two families with 46,XY DSD to the long arm of chromosome 5 with a combined, multipoint par

169 of a whole chromosome 5 or a deletion of the long arm of chromosome 5, -5/del(5q), is a recurring abn

170 htly linked to the Msx2 homeobox gene on the long arm of chromosome 5, and that affected individuals

171 ring interstitial loss of all or part of the long arm of chromosome 5, del(5q), is a hallmark of myel

172 Partial deletion of the long arm of chromosome 5, del(5q), is the cytogenetic ha

173 e scan localized the disease interval to the long arm of chromosome 5, with a maximum two-point param

174 ients, while 4 had a deletion of part of the long arm of chromosome 5.

175 chTRF1 gene was localized on the long arm of chromosome 5.

176 map of one highly recombinant region on the long arm of chromosome 5B.

177 ed by the expression of the Ph1 locus on the long arm of chromosome 5B.

178 omosome 4F with barley chromosome 4H and the long arm of chromosome 5H.

179 Deletion of the long arm of chromosome 6 (6q) is one of the most common

180 After stringency washes, the entire long arm of chromosome 6 (6q) was microdissected.

181 , including duplications of a portion of the long arm of chromosome 6 and uniparental disomy, implica

182 ion, the human MCH-2R gene was mapped to the long arm of chromosome 6 at band 6q16.2-16.3, a region r

183 equent deletions of the distal region on the long arm of chromosome 6 have been reported in multiple

184 Though deletion of the long arm of chromosome 6 is one of the most common aberr

185 A genomewide scan identified a region on the long arm of chromosome 6 that is significantly associate

186 es (TBP AND PSMB1) are tightly linked on the long arm of chromosome 6, in a region syntenic with the

187 d nonrandom chromosomal abnormalities of the long arm of chromosome 6.

188 h lung cancer are frequently observed in the long arm of chromosome 6.

189 of patients with WM harbour deletions in the long arm of chromosome 6.

190 Complete or partial deletions of the long arm of chromosome 7 (7q- and -7) are nonrandom abno

191 Deletions involving the long arm of chromosome 7 have not been described in RCCs

192 During the sequencing of the long arm of chromosome 7 in the Human Genome Project, a

193 sor in acute leukemias with deletions of the long arm of chromosome 7 or in other types of human mali

194 1 to 2 megabase deletion of a portion of the long arm of chromosome 7 that encompasses ELN.

195 from nine patients with abnormalities of the long arm of chromosome 7, and in each case one allele of

196 of heterozygosity for large portions of the long arm of chromosome 7, resulting in retention of only

197 the other quantitative trait locus is on the long arm of chromosome 7.

198 ons (EROs), have demonstrated linkage on the long arm of chromosome 7.

199 Gains in the long arm of chromosome 8 (8q) are believed to be associa

200 Allele loss from the long arm of chromosome 8 was also observed with 30.0% (6

201 5 loci on the short arm and one locus on the long arm of chromosome 8 were used for PCR-based LOH ana

202 mosomes due to an extra isochromosome of the long arm of chromosome 8, and the near-diploid karyotype

203 Slug maps to the long arm of chromosome 8, closely linked to D8S2090 betw

204 ydomonas reinhardtii, which we mapped to the long arm of chromosome 8, provides a good experimental s

205 ences contained within a "half-YAC" from the long arm of chromosome 8, that is, a YAC containing the

206 human alpha1B subunit gene, localized to the long arm of chromosome 9 (9q34) by fluorescence in situ

207 Allelic losses in the long arm of chromosome 9 are commonly encountered in man

208 Deletions of the long arm of chromosome 9 are the most common genetic alt

209 ported reassignment of marker BNL4053 to the long arm of chromosome 9.

210 reas 23-201 was located in the middle of the long arm of chromosome A2, suggesting the presence of se

211 homologous regions near the telomeres of the long arm of chromosome I and the short arm of chromosome

212 sod2 gene, located near the telomere on the long arm of chromosome I, encodes a Na+ (or Li+)/H+ anti

213 of the budding yeast genome, but not of the long arm of chromosome XII that contains the rDNA repeat

214 necessary to mediate the segregation of the long arm of chromosome XII.

215 The human GC-F gene was localized to the long arm of chromosome Xq22 by fluorescence in situ hybr

216 MCT-1 was localized to the long arm of chromosome Xq22-24 by flourescence in situ h

217 s 4 and 5, and paracentric inversions in the long arm of chromosomes 1 and 4; the latter is in a segm

218 In addition, we have localized AIM2 to the long arm of human chromosome 1 (band q22) in a highly co

219 the gene encoding Spalpha is located on the long arm of human chromosome 1 at q21-q23 within contig

220 studied loss of heterozygosity (LOH) on the long arm of human chromosome 18 in prostate cancer to de

221 ing to a region of about 500-kb pairs on the long arm of human chromosome 19 at q13.3.

222 oximal portion of mouse chromosome 7 and the long arm of human chromosome 19.

223 rogressive retinitis pigmentosa, maps to the long arm of human chromosome 1q41 between markers AFM268

224 osome 1 shares a region of homology with the long arm of human chromosome 2, suggesting that the huma

225 l genes form a cluster with the IL-1s on the long arm of human chromosome 2.

226 aining at least 40 genes that now map to the long arm of human chromosome 20.

227 DS results from an extra copy of the long arm of human chromosome 21 (HSA21) and the increase

228 Segments of the long arm of human chromosome 21 are conserved, centromer

229 -Mb nonrecombinant region of interest on the long arm of human chromosome 21, with a multipoint logar

230 the features of meiotic recombination on the long arm of human chromosome 21.

231 old sores is associated with a region on the long arm of human chromosome 21.

232 get of chromosomal aberrations involving the long arm of human chromosome 3 and is thereby inactivate

233 Rearrangements of the long arm of human chromosome 3, including reciprocal tra

234 hybrid mapping localized human CLOCK to the long arm of human chromosome 4 (4q12).

235 se has suggestive evidence of linkage to the long arm of human chromosome 4 (LOD score of 2.0) in a f

236 in a large Italian kindred is located on the long arm of human chromosome 4.

237 estigate the impact of the distal end of the long arm of human chromosome 5 (chromosomal region 5q31.

238 Loss of all or part of the long arm of human chromosome 5 is a recurrent abnormalit

239 a 35-Mb portion of the distal region of the long arm of human chromosome 5, q21-q35, was produced us

240 is caused by an interstitial deletion of the long arm of human chromosome 5.

241 h 13 microsatellite markers specific for the long arm of human chromosome 7 within 7q31; this region

242 Conserved gene order between CFA29 and the long arm of human chromosome 8 argued for homology betwe

243 roximately 20% of the physical length of the long arm of maize chromosome 1 is represented by a singl

244 map at 15q25 of human chromosome 15 and the long arm of mouse chromosome 7, respectively, each havin

245 BACs were FISH mapped, and paint the entire long arm of SSCY.

246 w chromosome-associated protein named LAB-1 (Long Arm of the Bivalent).

247 the pericentromeric region of the short and long arm of the chromosome.

248 landmark framework map over 20-25 Mb of the long arm of the human X chromosome using yeast artificia

249 S287, approximately 15-17 Mb of the proximal long arm of the human X chromosome.

250 Deletions of the AZFa region on the long arm of the human Y chromosome cause male infertilit

251 The DAZ gene on the long arm of the human Y chromosome is a strong candidate

252 gnosis of POF, we established linkage to the long arm of the X chromosome (between Xq21.1 and Xq21.3.

253 editary prostate cancer (termed HPCX) to the long arm of the X chromosome (Xq25-q27) through a genome

254 atellite BM4604, mapped to the middle of the long arm of the X chromosome at q26-q31.

255 lite INRA3O, mapped to the distal end of the long arm of the X chromosome at q42-ter and to the short

256 sically mapped DD44 to the distal end of the long arm of the X chromosome using fluorescence in situ

257 n the gene DKC1 in band 2, sub-band 8 of the long arm of the X chromosome.

258 -tagged site (STS)/YAC-based coverage of the long arm of the X chromosome.

259 6 were located on the short arm and 3 on the long arm of the X chromosome.

260 with a CGG expansion in the FMR1 gene on the long arm of the X chromosome.

261 chromatic regions around centromeres and the long arm of the Y chromosome, reduced growth capacity, a

262 gene or gene complex normally located on the long arm of the Y chromosome.

263 Recombination between markers on the long arm of this chromosome was completely eliminated, s

264 and 3363 BACs providing >85% coverage of the long arm of this chromosome.

265 onstruct a new sequence-ready BAC map of the long arm of this chromosome.

266 omeric heterochromatin to euchromatin on the long arm of this chromosome.

267 separated by gaps totalling 320 kb span the long arm of this metacentric chromosome.

268 e sequences were unambiguously mapped on the long arm of tomato SC 11.

269 me 5 and between the proximal portion of the long arm of wheat consensus chromosome 1 and rice chromo

270 effects were mapped as Mendelian loci on the long arms of Ae. speltoides chromosomes 3S and 7S.

271 of T. monococcum chromosomes 1 and 5 and the long arms of barley chromosomes 2 and 3.

272 lit into two main locations on the short and long arms of chromosome 6.

273 by a reciprocal translocation involving the long arms of chromosomes 4 and 5, and paracentric invers

274 romosome 3, which is known to be syntenic to long arms of group-4 chromosomes of wheat.

275 ive percent of these 1918 loci mapped to the long arms of homoeologous group 4 chromosomes, while 35%

276 found with polymorphic loci that map to the long arms of human chromosomes 20 and 12 in regions cont

277 from chromosomal domains referred to as the long arms of the bivalents.

278 omes and map to orthologous positions on the long arms of the group 5 chromosomes.

279 autosomal region 2 (PAR2) at the tips of the long arms of the X and Y chromosomes is thought to have

280 s involved loss of the whole, or part of the long arm, of chromosome 22.

281 of loss in chromosome 5q31.1 (chromosome 5, long arm, region 3, band 1, subband 1) in myelodysplasia

282 Three alleles of the kl-3 gene on the Y long arm result in loss of the axonemal outer dynein arm

283 -homologous region close to the end of the X long arm, spanning three X BACs.

284 The number of EST loci was greater on the long arms than on the short arms for all three chromosom

285 Three times more loci were mapped on the long arms than on the short arms, and a significantly hi

286 ms the most and in the distal regions of the long arms the least.

287 recombination in the proximal regions of the long arms the most and in the distal regions of the long

288 tivity in G1-G3 is cryptic in intact laminin long arm, the active heparin binding site of G domain ap

289 e added to this genotype, thus supplying the long arm, the inactive centromere regained the property

290 ecreased in stepwise fashion from the distal long arm to the distal short arm in at least four "evolu

291 n both cases, high-resolution banding of the long arm was normal, and FISH of probes D15S11, SNRPN, D

292 size and lies in the distal one-third of the long arm, where the pseudoautosomal region (PAR) is loca

293 n the distal short arm and one on the distal long arm, whereas acrocentric chromosomes exhibit a sing

294 l and included globules with a foreshortened long arm, while the trimeric species has the typical fou

295 s was mapped to two potential regions on the long arm with an intervening recombination.

296 ble for the variable skewing to the proximal long arm (Xq12-q22) of the X chromosome (Z=5.7, P=.002,

297 We examined the long arm XY pseudoautosomal region for linkage to asthma

298 The mouse Y long arm (Yq) carries hundreds of supposedly intronless

299 plex Ssty gene family present on the mouse Y long arm (Yq) has been implicated in sperm development,

300 ted exclusively on the short arm (Yp) or the long arm (Yq).