1 Deletions of the
short arm of chromosome 1 (1p) are the second most commo
2 Loss of the
short arm of chromosome 1 (1p) is the second most freque
3 s been cloned and positionally mapped to the
short arm of chromosome 1 (1p35-p31.3; refs 6-8).
4 Deletions of the distal
short arm of chromosome 1 (1p36) represent a common, new
5 LC3B) for primary congenital glaucoma to the
short arm of chromosome 1 (1p36.2-36.1) that is situated
6 Ablation of the distal end of the
short arm of chromosome 1 [1p36 deletion syndrome (1p36D
7 enase mutation; (b) the combined loss of the
short arm of chromosome 1 and the long arm of chromosome
8 iptional profiling suggests that loss of the
short arm of chromosome 1 in cellular leiomyomata, an un
9 The distal
short arm of chromosome 1 is commonly deleted in a varie
10 Deletion of the distal
short arm of chromosome 1 occurs in 35% of primary neuro
11 ntified an approximately 50-Mb region on the
short arm of chromosome 1 where patterns of polymorphism
12 kage map positions 0.0-81.8 cM reside in the
short arm of chromosome 1 whereas markers from 81.8-242.
13 We have identified a region on the
short arm of chromosome 1 which is frequently deleted in
14 This gene, called p73, maps to the
short arm of chromosome 1, and is found in a region that
15 The human mutY gene maps on the
short arm of chromosome 1, between p32.1 and p34.3.
16 UL characterized by loss of a portion of the
short arm of chromosome 1, clustered with malignant leio
17 posterior polar cataract (CPP) to the distal
short arm of chromosome 1.
18 cted for the initial screening of the entire
short arm of chromosome 1.
19 frequent loss of heterozygosity (LOH) on the
short arm of chromosome 1.
20 roto-oncogene and loss of all or part of the
short arm of chromosome #
1 are both associated with a po
21 The
short arm of chromosome 10 was not affected.
22 d a single locus for the disease gene on the
short arm of chromosome 10 with a maximum 2-point lod sc
23 esporial cells1 (mac1) and located it to the
short arm of chromosome 10.
24 vel gene responsible for ARVD resides on the
short arm of chromosome 10.
25 yndrome caused by a proximal deletion in the
short arm of chromosome 11 (Potocki-Shaffer syndrome).
26 PSMA/GCPII is located on the
short arm of chromosome 11 and functions as both a folat
27 Loss of heterozygosity (LOH) on the
short arm of chromosome 11 is the most frequent genetic
28 An initial report of linkage on the
short arm of chromosome 11 was revised and remains unrep
29 -Weidemann syndrome of the BWS region on the
short arm of chromosome 11.
30 on was an isolated gain involving the entire
short arm of chromosome 11.
31 Gain of the
short arm of chromosome 12 detected in almost all adult
32 d nonrandom chromosomal abnormalities of the
short arm of chromosome 12.
33 12.1 and seven TGCTs with gain of the entire
short arm of chromosome 12.
34 -related gene (EEG-1) that is located on the
short arm of chromosome 12.
35 re 3.4) was found 161 cM from the tip of the
short arm of chromosome 12; these results were confirmed
36 Excess allele sharing was found on the
short arm of chromosome 16 and confirmed by conventional
37 that the human COX6AH gene is located on the
short arm of chromosome 16 and facilitated the isolation
38 d a subtelomeric rearrangement involving the
short arm of chromosome 16 that gives rise to alpha-thal
39 g from the terminal (TTAGGG)n repeats of the
short arm of chromosome 16, providing a full description
40 alpha-globin complex lies at the tip of the
short arm of chromosome 16.
41 ur suppressor protein p53, is located on the
short arm of chromosome 17 (17p).
42 e chromosomes localized the Tnk1 gene to the
short arm of chromosome 17 (17p13.1), near the p53 locus
43 idence for linkage of fasting insulin to the
short arm of chromosome 17 (logarithm of odds [LOD] = 3.
44 The
short arm of chromosome 17 has emerged as a hot spot whe
45 e observed frequent loss of sequences on the
short arm of chromosome 17 in the region of the TP53 gen
46 nd cytogenetic abnormalities of the proximal
short arm of chromosome 17 include Charcot-Marie-Tooth d
47 ce expression, heterozygous deletions of the
short arm of chromosome 17, and mutations in IDH1/IDH2 a
48 cus, a commonly used telomeric marker on the
short arm of chromosome 17.
49 omal dominant anterior polar cataract on the
short arm of chromosome 17.
50 nce of 14 loci in the proximal region of the
short arm of chromosome 17.
51 of LG 9 and LG 13 and localized them to the
short arm of chromosome 17.
52 MT, is caused by a 1.5 Mb duplication on the
short arm of chromosome 17.
53 more potential tumor suppressor genes on the
short arm of chromosome 18 which may be involved in NSCL
54 most tumors lose heterozygosity only on the
short arm of chromosome 18.
55 Here we performed fine mapping of the
short arm of chromosome 19 and found that the LKB1/STK11
56 20 encoding TCblR is located at p13.2 on the
short arm of chromosome 19, spans a length of 6.224 kb,
57 b genome) to a ditelosomic stock missing the
short arm of chromosome 1B (1BS) and wheat-rye transloca
58 Alterations of the
short arm of chromosome 2 (2p) have been of particular i
59 inkage was obtained for three markers on the
short arm of chromosome 2 (2p16), with a maximum two-poi
60 responsible for Carney complex map(s) to the
short arm of chromosome 2 (2p16).
61 cant genetic evidence for a MED locus on the
short arm of chromosome 2 (2p24-p23), and a search for c
62 d significant linkage to nine markers on the
short arm of chromosome 2, a region overlapping that rec
63 Both mel1 and snm1 map to the
short arm of chromosome 2, and snm2 maps to the long arm
64 -kb mtDNA into the pericentric region on the
short arm of chromosome 2.
65 ult of a complex rearrangement involving the
short arm of chromosome 2.
66 nase (ALK), generated by an inversion on the
short arm of chromosome 2: inv(2)(p21p23).
67 wy body-confirmed Parkinson's disease on the
short arm of chromosome 20 (20pter-p12) and identify TME
68 Linkage to the
short arm of chromosome 20 in a genome screen was follow
69 enetically mapped to overlapping loci on the
short arm of chromosome 20.
70 The gene maps near the telomere on the
short arm of chromosomes 2A, 2B, and 2D.
71 Allelic deletion of multiple regions on the
short arm of chromosome 3 (3p) implies the presence of m
72 n, shows a deletion of gene sequences in the
short arm of chromosome 3 (3p) in as many as 100% of cas
73 Allelic deletions involving the
short arm of chromosome 3 (3p13-21.1) have been observed
74 The hOGG1 gene is localized on the
short arm of chromosome 3 (3p25/26) in a region commonly
75 ing the loss of the telomeric portion of the
short arm of chromosome 3 and characterized by developme
76 Loss of heterozygosity involving the
short arm of chromosome 3 has been reported in gastric a
77 The
short arm of chromosome 3 has been shown to exhibit high
78 lms' tumor, and loss or rearrangement of the
short arm of chromosome 3 in clear and chromophobe RCC.
79 High frequencies of allelic loss on the
short arm of chromosome 3 in small cell lung cancer (SCL
80 Loss of heterozygosity within the
short arm of chromosome 3 is a common molecular event in
81 ehydrogenase-2, whereas another locus on the
short arm of chromosome 3 is linked with a cytosolic tri
82 Allelic loss at the
short arm of chromosome 3 is one of the most common and
83 The
short arm of chromosome 3 is thought to harbor a novel o
84 Deletions within the
short arm of chromosome 3 occur very frequently in human
85 Loss of heterozygosity at the
short arm of chromosome 3 occurs frequently in head and
86 ) has been correlated with a deletion in the
short arm of chromosome 3, with the region 3p21 being lo
87 tion of the VHL tumor suppressor gene on the
short arm of chromosome 3.
88 ion of the VHL tumour suppressor gene on the
short arm of chromosome 3.
89 implicated a tumor suppressor gene(s) on the
short arm of chromosome 3.
90 entity caused by a terminal deletion of the
short arm of chromosome 4 (4p-).
91 order associated with the distal part of the
short arm of chromosome 4 (4p16.3).
92 One of these is on the
short arm of chromosome 4 and is linked with a cluster o
93 nes and conserved unannotated regions on the
short arm of chromosome 4 from Arabidopsis were experime
94 resulting from a hemizygous deletion of the
short arm of chromosome 4, called the WHS critical regio
95 e same location as the bxbx mutation, on the
short arm of chromosome 4.
96 is encoded by a single gene that maps to the
short arm of chromosome 4.
97 is caused by sub-telomeric deletions in the
short arm of chromosome 4.
98 d unstable trinucleotide (CAG) repeat on the
short arm of chromosome 4.
99 ely in centromeric regions as well as on the
short arms of chromosomes 4 and 10.
100 All ecotypes contain 5S rDNA in the
short arms of chromosomes 4 and 5.
101 aize plants that are trisomic for 90% of the
short arm of chromosome 5 and monosomic for a small dist
102 ihydrate deposition disease, a region on the
short arm of chromosome 5 was found to be genetically li
103 esistance to this disease are located on the
short arm of chromosome 5(1H).
104 s been localized to a 0.8-cM interval on the
short arm of chromosome 5, between the polymorphic micro
105 omeobox gene knox10, which is located on the
short arm of chromosome 5, was shown to be ectopically e
106 The gene was mapped to the
short arm of chromosome 5D and mediated recognition of t
107 A QTL with a minor effect was mapped on the
short arm of chromosome 5S and was designated QPh.ucd-5S
108 Allelic deletions on the
short arm of chromosome 6 (6p) are one of the common, po
109 96, HFE, the gene for HHC, was mapped on the
short arm of chromosome 6 (6p21.3).
110 monosomic for a small distal portion of the
short arm of chromosome 6 exhibited a phenotypic syndrom
111 additional QTL, represented by umc85 on the
short arm of chromosome 6, affected antibiosis (R2 = 15.
112 9 in Solanum arcanum accession LA2157 to the
short arm of chromosome 6, in a genetic interval as Mi-1
113 LA) complex, a dense cluster of genes on the
short arm of chromosome 6, was first noted over 30 years
114 etween the markers RM19291 and RM8072 on the
short arm of chromosome 6, where a gene for resistance t
115 (PSORS1, Psoriasis Susceptibility 1), on the
short arm of chromosome 6.
116 quantitative-trait locus (QTL) for RD on the
short arm of chromosome 6.
117 tative quantitative-trait locus (QTL) on the
short arm of chromosome 6.
118 physically map barley genes to the long and
short arms of chromosome 6(6H).
119 Linkage to the
short arm of chromosome 7 at 7p14 was found using the ma
120 The gene is located on the
short arm of chromosome 7.
121 TA-ACS1 is located on the
short arm of chromosomes 7A and 7D and on the long arm o
122 Allelic losses on the
short arm of chromosome 8 (8p) have been reported as fre
123 in hepatocellular carcinoma (HCC) is of the
short arm of chromosome 8 (8p).
124 ar the lipoprotein lipase (LPL) locus on the
short arm of chromosome 8 (P = 0.002, n = 125 sib-pairs,
125 umor exhibits loss of heterozygosity for the
short arm of chromosome 8 and has a complex karyotype.
126 Deletions on the
short arm of chromosome 8 are recurrent in liver, breast
127 ltiple lines of evidence have implicated the
short arm of chromosome 8 as harboring genes important i
128 Numerous studies have implicated the
short arm of chromosome 8 as the site of one or more tum
129 crosses the translocation breakpoint on the
short arm of chromosome 8 in this patient.
130 The
short arm of chromosome 8 is frequently lost in epitheli
131 Many epithelial tumors show deletion of the
short arm of chromosome 8 that is related to aggressive
132 The
short arm of chromosome 8, 8p, is often rearranged in ca
133 8% identical to TrnR1, and is located on the
short arm of chromosome 8.
134 ostate cancer (HPC), using 24 markers on the
short arm of chromosome 8.
135 alterations at 15 microsatellite loci on the
short arm of chromosome 8.
136 Deletion of the distal
short arm of chromosome 9 (9p) has been reported in a nu
137 encoding interferon-kappa is located on the
short arm of chromosome 9 adjacent to the type I interfe
138 tence of other tumor suppressor genes on the
short arm of chromosome 9 in SCLC, we tested 46 primary
139 The data identify a homozygous loss on the
short arm of chromosome 9 suggesting the presence of a n
140 s, translocated from the B chromosome to the
short arm of chromosome 9 was recently found to be epige
141 DMT1 maps to the distal
short arm of chromosome 9, a location implicated in huma
142 ning gene to the very terminal region of the
short arm of chromosome 9.
143 centromere that had been translocated to the
short arm of chromosome 9.
144 eres of the long arm of chromosome I and the
short arm of chromosome II.
145 The gene maps to the
short arm of chromosome one in the rat.
146 in close proximity to the HLA region on the
short arm of chromosome six.
147 in a major disease-resistance cluster on the
short arm of chromosome V, including the R1 resistance (