ライフサイエンスコーパス: cleft lip

1 BMI change was not related to the risk of cleft lip.

2 tin cre transgenic line resulted in isolated cleft lip.

3 tic attenuation results in failed fusion and cleft lip.

4 number of realistic facial images depicting cleft lip.

5 that disruption of this sequence results in cleft lip.

6 been identified in both mice and humans with cleft lip.

7 ed by persistence of the epithelial seam and cleft lip.

8 tches in the upper beak or the equivalent of cleft lip.

9 outgrowth, epithelial seam persistence, and cleft lip.

10 Cases were infants with isolated defects--cleft lip alone (n = 334), cleft lip and palate (n = 494

11 haled steroids were confirmed (cleft palate, cleft lip, anal atresia, and hypospadias).

12 beta2-agonists were found for spina bifida, cleft lip, anal atresia, severe congenital heart defects

13 ndwork for understanding the causes of human cleft lip and analyzing the mechanism of action of growt

14 the result is orofacial clefting, including cleft lip and cleft palate (CL/P).

15 Cleft lip and cleft palate (CLP) are common disorders th

16 Three common diseases, isolated cleft lip and cleft palate (CLP), hypothyroidism and thy

17 Because cleft lip and cleft palate do not frequently co-aggregat

18 Wnt9b mutations are associated with cleft lip and cleft palate in mice; however, the cause o

19 features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.

20 the molecular pathogenesis of the bilateral cleft lip and cleft palate that results from mutation of

21 Among individuals with isolated cleft lip and cleft palate, increased risks of intellect

22 t between the facial processes that leads to cleft lip and cleft palate.

23 ork has focused on the molecular etiology of cleft lip and clefts of the hard palate, but study of th

24 surgical outcome assessment in patients with cleft lip and for the rehabilitation of patients with fa

25 Cleft lip and other congenital anomalies are also linked

26 Orofacial clefts, including cleft lip and palate (CL/P) and neural tube defects (NTD

27 Cleft lip and palate (CL/P) is a common disfiguring birt

28 also observed wider de novo deletions among cleft lip and palate (CLP) cases than seen among cleft p

29 notypic spectrum - including cleft lip (CL), cleft lip and palate (CLP), or cleft palate (CP) - and c

30 d MAFB and isolated cleft lip only (CLO) and cleft lip and palate (CLP).

31 isolated defects--cleft lip alone (n = 334), cleft lip and palate (n = 494), or cleft palate alone (n

32 Nonsyndromic cleft lip and palate (NS CLP) is a complex birth defect

33 shortened fifth fingers (one), microtia with cleft lip and palate (one), microtia alone (one), and ne

34 ormations (RR, 1.52; 95% CI, 1.02-2.25), and cleft lip and palate (RR, 3.23; 95% CI, 1.44-7.22) compa

35 patients with surgically repaired unilateral cleft lip and palate (UCLP) undergoing orthodontic corre

36 amilies with autosomal dominant nonsyndromic cleft lip and palate and 3 families with autosomal domin

37 We studied a patient with isolated cleft lip and palate and a balanced chromosomal transloc

38 syndrome (VWS) is a common form of syndromic cleft lip and palate and accounts for approximately 2% o

39 tudies showed that mutations in IRF6 lead to cleft lip and palate and mandibular abnormalities.

40 ed from MMF to SRL during late pregnancy had cleft lip and palate and microtia) and three SA.

41 ere craniofacial defects including bilateral cleft lip and palate and tongue agenesis, following the

42 r teeth alignment; Group 3 had patients with cleft lip and palate but no treatment for teeth alignmen

43 ate and accounts for approximately 2% of all cleft lip and palate cases.

44 These mutants developed median cleft lip and palate demonstrating a previously undocume

45 Seventeen percent of those with cleft lip and palate had another defect compared with 9%

46 Cleft lip and palate have a complex inheritance, and 90%

47 y drain saliva, and patients with the common cleft lip and palate have a higher prevalence of dental

48 ions (p = 0.001), and with SNP rs3923086 and cleft lip and palate in Asian populations (p = 0.004).

49 signaling pathway have been associated with cleft lip and palate in humans and mice, the mechanisms

50 Cleft lip and palate is a common human birth defect, and

51 most recent advances in the understanding of cleft lip and palate occurrence.

52 15 cleft lip and palate organisations totalled 26% of both

53 Recently, we identified a family in which cleft lip and palate segregated in two of three generati

54 surgery such as ophthalmology (88, 28%) and cleft lip and palate surgery (70, 22%) were also frequen

55 s are directed at ophthalmology, followed by cleft lip and palate surgery.

56 Cleft lip and palate syndromes are among the most common

57 Cleft lip and palate syndromes in humans are associated

58 For boys, the risk was greater for cleft lip and palate than for cleft lip only (odds ratio

59 Cleft lip and palate transmembrane protein 1 (Clptm1) is

60 Here, we identify cleft lip and palate transmembrane protein 1-like protei

61 Patients with cleft lip and palate undergoing treatment with fixed bra

62 health and microbial flora in patients with cleft lip and palate undergoing treatment with fixed bra

63 alformation, other cardiac malformation, and cleft lip and palate was higher for infants exposed to T

64 20 patients with complete unilateral cleft lip and palate were prospectively recruited.

65 he disorder is an autosomal dominant form of cleft lip and palate with lip pits, and is the most comm

66 a positive dose response among infants with cleft lip and palate+ (for light smokers, odds ratio (OR

67 ditional malformations: cleft lip+ (n = 58), cleft lip and palate+ (n = 140), or cleft palate+ (n = 2

68 aking and aid in treating conditions such as cleft lip and palate, among other congenital craniofacia

69 tations in several candidate genes may cause cleft lip and palate, but definitive evidence regarding

70 been shown to be an important contributor to cleft lip and palate, but the functional variant leading

71 s are candidate genes for genetic disorders (cleft lip and palate, certain forms of cancer) or solute

72 ed with syndromic and non-syndromic forms of cleft lip and palate, consistent with a role for Irf6 in

73 The proband presented with bilateral cleft lip and palate, malformed auricles, and bilateral

74 es a constellation of abnormalities, such as cleft lip and palate, pigmentary retinopathy, and multip

75 petitive urinary tract infections, bilateral cleft lip and palate, retinopathy, and gut malrotation.

76 involvement in an autosomal dominant form of cleft lip and palate, Van der Woude's syndrome.

77 The risk of cleft lip only, but not of cleft lip and palate, was increased for twins (odds rati

78 ily of three affected siblings with isolated cleft lip and palate, we discovered that they share a no

79 nomalies and facial dysmorphology, including cleft lip and palate.

80 he FGF family has also been shown to lead to cleft lip and palate.

81 on the current knowledge of the etiology of cleft lip and palate.

82 variation in IRF6 confers risk for isolated cleft lip and palate.

83 factor Esrp1 have fully penetrant bilateral cleft lip and palate.

84 th a cleft palate only, and 534 (44.6%) with cleft lip and palate.

85 eal pterygium syndrome, 2 syndromic forms of cleft lip and palate.

86 d to improve nasal symmetry in patients with cleft lip and palate.

87 th prolonged treatment trajectories, such as cleft lip and palate.

88 rimary cilium, and these patients often have cleft lip and palate.

89 splicing regulatory protein (Esrp1) develop cleft lip and palate.

90 ome (VWS), the most common syndromic form of cleft lip and palate.

91 upracondylar fracture of humerus: ICC, 0.25; cleft lip and palate: ICC, 0.24; acute appendicitis with

92 ophic nails, hypodontia, ankyloblepharon and cleft lip and/or cleft palate.

93 detected in the DNA of 74 unrelated cases of cleft lip and/or cleft palate; no variants associated si

94 Cleft lip and/or palate (CL/P) are common anomalies occu

95 Cleft lip and/or palate (CL/P) are common structural bir

96 Cleft lip and/or palate (CL/P) is the most common cranio

97 In Ethiopia, more than 70% of infants with cleft lip and/or palate (CL/P) lack access to surgery.

98 Cleft lip and/or palate (CL/P), the most frequent human

99 lex aetiology and the variable penetrance of cleft lip and/or palate (CL/P), understanding the molecu

100 atypical orofacial clefts and with syndromic cleft lip and/or palate (CL/P).

101 Patients with cleft lip and/or palate (CLP), who undergo numerous medi

102 Nonsyndromic cleft lip and/or palate (NSCL/P) is a prevalent birth de

103 Non-syndromic cleft lip and/or palate (NSCLP) is a common congenital m

104 Nonsyndromic Cleft Lip and/or Palate (NSCLP) is regarded as a multifa

105 l and known candidate genes for nonsyndromic cleft lip and/or palate through genome-wide linkage anal

106 tes the genetic contribution to nonsyndromic cleft lip and/or palate through the analysis of family p

107 by bilateral choanal atresia, hearing loss, cleft lip and/or palate, and other craniofacial dysmorph

108 r because of abnormal development (including cleft lip and/or palate, craniosynostosis and facial dys

109 including characteristic facial dysmorphism, cleft lip and/or palate, craniosynostosis, learning disa

110 857 806 newborns included, 1197 (0.1%) had a cleft lip and/or palate, including 170 (14.2%) with a cl

111 expression of genes previously implicated in cleft lip and/or palate, including components of multipl

112 Anomalies, such as cleft lips and palates, were more frequent in females, w

113 NCC knockout embryos showed fully penetrant cleft lips and short snouts.

114 l tube defects to neurocristopathies such as cleft-lip and cleft-palate, cardiac septal defects, and

115 ults obtained using phenytoin (which induces cleft lip) and 6-aminonicotinamide (which induces cleft

116 at govern lip morphogenesis nor the cause of cleft lip are well understood.

117 The cleft lip area, bilateral nostril areas, and the nostril

118 rther investigated the mechanisms leading to cleft lip as well as cleft palate in both existing and n

119 Twenty-eight fetuses had a cleft lip at birth.

120 milies with NSCL/P, in particular those with cleft lip but not cleft palate.

121 others of limb deficiency, cleft palate, and cleft lip cases were, respectively, 1.8 (95% CI: 1.1, 3.

122 We named this new Mendelian syndrome CATIFA (cleft lip, cataract, tooth abnormality, intellectual dis

123 cases than seen among cleft palate (CP) and cleft lip (CL) cases.

124 cur across a phenotypic spectrum - including cleft lip (CL), cleft lip and palate (CLP), or cleft pal

125 s who consumed alcohol tended to be near to (cleft lip, cleft lip with cleft palate) or to exceed (cl

126 Orofacial clefts (cleft lip, cleft palate) are among the most common of al

127 tralogy of Fallot, coarctation of the aorta, cleft lip, cleft palate, anorectal atresia/stenosis, and

128 Cases with a cleft lip, cleft palate, or both and unaffected controls

129 We apply our method to data on cleft lip/cleft palate and schizophrenia.

130 uced by the method of Farrall and Holder for cleft lip/cleft palate data is not consistent with the p

131 ratosis and onychodysplasia, syndactyly, and cleft lip/cleft palate.

132 t disorders characterized by combinations of cleft lip, CLP, lip pits, skin-folds, syndactyly and ora

133 showcase DOT by analyzing breast cancer and cleft lip data, in which our method strengthened levels

134 Cleft lip defects are usually regarded as a single entit

135 rs of unique faces depicting a wide range of cleft lip deformity with variation of ethnic background.

136 rter snout, expansion of the facial midline, cleft lip, extensive exencephaly, and microphthalmia or

137 t MSX1 mutations could increase the risk for cleft lip formation by interacting with an impaired morp

138 uals with isolated cleft palate (ie, without cleft lip) had increased mortality (hazard ratio, 3.4; 9

139 interesting because the occurrence of fetal cleft lip has been demonstrated to increase with materna

140 Cleft lip has previously been described in one individua

141 f a large multi-ethnic human population with cleft lip identified clusters of single-nucleotide polym

142 osome 4, inv(4)(p13q21) that segregates with cleft lip in a two-generation family.

143 Cleft lip is one of the most common human birth defects,

144 Cleft lip is one of the most common human birth defects.

145 l defects, middle-ear defects, cleft palate, cleft lip, limb defects, limb-reduction defects, polydac

146 th clefts plus (+) additional malformations: cleft lip+ (n = 58), cleft lip and palate+ (n = 140), or

147 ct of the A allele, with a relative risk for cleft lip of 1.68 for the AG genotype and 2.40 for the A

148 , 8q24, KIAA1598-VAX1, and MAFB and isolated cleft lip only (CLO) and cleft lip and palate (CLP).

149 c orofacial clefts (NSOFCs) are nonsyndromic cleft lip only (NSCLO), nonsyndromic cleft lip with pala

150 as greater for cleft lip and palate than for cleft lip only (odds ratio=2.4 vs. 1.8, p<0.001 for diff

151 They assessed the distribution of cleft lip only and cleft lip with cleft palate by covari

152 ce: Young adults who were born with isolated cleft lip only did not differ significantly from unaffec

153 With likelihood ratio test analysis, "cleft lip only" showed association with MSX1 (p = 0.04)

154 GEF19 (cleft lip with/without palate), FBN2 (cleft lip only), SLC35B3 (cleft palate only), CASC20 (Pi

155 and/or palate, including 170 (14.2%) with a cleft lip only, 493 (41.2%) with a cleft palate only, an

156 The risk of cleft lip only, but not of cleft lip and palate, was inc

157 nother defect compared with 9% of those with cleft lip only.

158 t lip with cleft palate and 1,122 cases with cleft lip only.

159 5%CIs1.50-6.59, p = 0.03) than children with cleft lip only.

160 ity or mortality among persons with isolated cleft lip only.

161 ), hypospadias (0.6%), hydrocephalus (0.6%), cleft lip or palate (0%), and obstetric fistula (0%).

162 Cleft lip or palate (or the two in combination) is a com

163 or 12 percent of the genetic contribution to cleft lip or palate and tripled the risk of recurrence i

164 Prevalent diagnosis of a cleft lip or palate at birth.

165 Additionally, children with cleft lip or palate had a substantial increase in odds o

166 Cleft lip or palate is a prevalent birth defect, occurri

167 contribution of variants in single genes to cleft lip or palate is an important consideration in gen

168 Median CERs of cleft lip or palate repair ($47.74 per DALY), general su

169 During the 2-year follow-up, children with a cleft lip or palate showed higher incidence rate ratios

170 control analyses, and determined the risk of cleft lip or palate that is associated with genetic vari

171 his nationwide cohort study, the presence of cleft lip or palate was associated with increased hospit

172 Newborns with cleft lip or palate were more likely to be male (55.8% v

173 escended testes, hypospadias, hydrocephalus, cleft lip or palate, and club foot.

174 ts, and is the most common syndromic form of cleft lip or palate.

175 g the first 2 years of life in newborns with cleft lip or palate.

176 Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome is a debilitating genode

177 enesis is commonly found in individuals with cleft lip/palate (CL/P), we used four large cohorts to e

178 Patients with cleft lip/palate (CLP) have been reported, in some studi

179 Cleft lip/palate (CLP), the most common craniofacial mal

180 ith both syndromic and nonsyndromic forms of cleft lip/palate (CLP).

181 hem, ectrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) syndrome is caused by single poin

182 from ectrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) syndrome patients with p63 mutati

183 cause the ectodermal dysplasia-ectrodactyly-cleft lip/palate (EEC) syndrome, comprising SHFM.

184 ns found in ectrodactylyectodermal dysplasia-cleft lip/palate (EEC), Limb-mammary syndrome (LMS) and

185 example ectrodactyly--ectodermal dysplasia--cleft lip/palate (EEC; OMIM 604292), limb--mammary syndr

186 a notably higher prevalence among those with cleft lip/palate and dentofacial deformities.

187 ofacial phenotypes such as craniosynostosis, cleft lip/palate and micrognathia.

188 yposmia; and (iii) Q680X in a nIHH male with cleft lip/palate and missing teeth, his brother with nIH

189 dence of the involvement of chromosome 6q in cleft lip/palate and suggest PRSS35 as a novel candidate

190 Patients with repaired cleft lip/palate had fewer mean movements than control i

191 Recent studies of cleft lip/palate have shown the association of genes inv

192 association of PRSS35 and SNAP91 genes with cleft lip/palate in the case-control cohort and in Cauca

193 Cleft lip/palate is a defect of craniofacial development

194 Since cleft lip/palate is also associated with both tooth agen

195 p revision surgery in patients with repaired cleft lip/palate is based on surgeons' subjective evalua

196 are linked to mental retardation (MR) and a cleft lip/palate phenotype.

197 To investigate if genes associated with cleft lip/palate were also associated with oral cancer,

198 escended testes, hypospadias, hydrocephalus, cleft lip/palate, and clubfoot) was determined by physic

199 lts in defects analogous to hypotelorism and cleft lip/palate, characteristics of the mild forms of h

200 urgically treatable conditions (breast mass, cleft lip/palate, club foot, hernia or hydrocele [adult

201 We identified a novel mouse mutant (cleft lip/palate, edema and exencephaly; Clpex) with a h

202 e been associated with cognitive defects and cleft lip/palate, its role in mammalian development and

203 representing 14 specialties (ophthalmology, cleft lip/palate, multidisciplinary teams, orthopaedics,

204 fferent surgical specialties (ophthalmology, cleft lip/palate, multidisciplinary teams, orthopaedics,

205 syndrome (ADULT; OMIM 103285) and recessive cleft lip/palate--ectodermal dysplasia (CLPED1; OMIM 225

206 th several types of cancer and recently with cleft lip/palate.

207 has been suggested as a candidate region for cleft lip/palate.

208 A total of 120 studies (41.9%) discussed cleft lip/palate.

209 this disorder; however, our understanding of cleft lip pathogenesis remains incomplete.

210 with the cellular mechanism demonstrated for cleft lip pathogenesis, we found that either SHH ligand

211 us mutants exhibit an incompletely penetrant cleft lip phenotype.

212 ementation in utero can partially rescue the cleft lip phenotype.

213 of the defect, epidemiologic assessments of cleft lip should, when possible, include separate analys

214 e identify CDH3 variants in individuals with cleft lip, supporting the relevance of this mechanism in

215 may influence future surgical approaches to cleft lip surgery.

216 e remain a limited number of mouse models of cleft lip that can be leveraged to characterize the gene

217 tributes to the etiology and pathogenesis of cleft lip through antagonistic interactions with other g

218 The location of the cleft lip was correctly identified in all fetuses with 3

219 formation, Msx1-deficient embryos develop a cleft lip when the mother is transiently exposed to redu

220 Cleft lip, which results from impaired facial process gr

221 th cleft lip who had revision, patients with cleft lip who did not, and non-cleft control individuals

222 d clinical trial that included patients with cleft lip who had revision, patients with cleft lip who

223 ear two genes not previously associated with cleft lip with and without cleft palate (MAFB, most sign

224 e used in a genome-wide association study of cleft lip with and without cleft palate.

225 GI, the authors identified associations with cleft lip with cleft palate (aOR = 1.23) and anorectal a

226 een 1967 and 1998, there were 1,572 cases of cleft lip with cleft palate and 1,122 cases with cleft l

227 essed the distribution of cleft lip only and cleft lip with cleft palate by covariate.

228 Although cleft lip with cleft palate may simply represent a more

229 Dental anomalies were more prevalent in cleft lip with cleft palate than other cleft types.

230 med alcohol tended to be near to (cleft lip, cleft lip with cleft palate) or to exceed (cleft palate)

231 Wnt/beta-catenin signaling pathway, leads to cleft lip with cleft palate.

232 MP4 and GREM1) specifically for nonsyndromic cleft lip with cleft palate.

233 2%), encephalocele (83%), cleft palate (0%), cleft lip with or without cleft palate (14%), omphalocel

234 hree or more occasions: odds ratio = 3.2 for cleft lip with or without cleft palate (95% confidence i

235 vitamins or liver consumption would decrease cleft lip with or without cleft palate (CL +/- P) risk a

236 udies suggest that the risks of nonsyndromic cleft lip with or without cleft palate (CL+/-P) and isol

237 tudies suggest that the risk of nonsyndromic cleft lip with or without cleft palate (CL+/-P) and isol

238 g mutations by screening 33 individuals with cleft lip with or without cleft palate (CL/P) and 19 ind

239 Nonsyndromic cleft lip with or without cleft palate (CL/P) and nonsyn

240 de linkage scan discovered a novel locus for cleft lip with or without cleft palate (CL/P) at 9q22-q3

241 Isolated or nonsyndromic cleft lip with or without cleft palate (CL/P) is a commo

242 Cleft lip with or without cleft palate (CL/P) is a commo

243 Cleft lip with or without cleft palate (CL/P) is a commo

244 Non-syndromic (NS) cleft lip with or without cleft palate (CL/P) is a commo

245 Previous work suggested that cleft lip with or without cleft palate (CL/P) is genetic

246 Cleft lip with or without cleft palate (CL/P) is one of

247 Oral facial cleft (OFC) comprises cleft lip with or without cleft palate (CL/P) or cleft p

248 a gene (TGFA) polymorphisms with the risk of cleft lip with or without cleft palate (CL/P) or cleft p

249 authors genotyped 244 infants with isolated cleft lip with or without cleft palate (CL/P), 99 with i

250 The etiology of cleft lip with or without cleft palate (CL/P), a common

251 l clefts (OFCs), which include non-syndromic cleft lip with or without cleft palate (CL/P), are among

252 palate (CP) is higher than that of isolated cleft lip with or without cleft palate (CL/P).

253 Non-syndromic cleft lip with or without cleft palate (CL/P, MIM 119530

254 f delivering infants with cleft palate (CP), cleft lip with or without cleft palate (CLP), conotrunca

255 increased risk of anencephaly, spina bifida, cleft lip with or without cleft palate (CLP), or cleft p

256 lefts (n = 303), cleft palate (n = 108), and cleft lip with or without cleft palate (n = 195).

257 identified in several GWAS for non-syndromic cleft lip with or without cleft palate (NS CL/P).

258 ndidate gene in the etiology of nonsyndromic cleft lip with or without cleft palate (NS-CL/P) and of

259 The majority (85%) of nonsyndromic cleft lip with or without cleft palate (nsCL/P) cases oc

260 n implicated in the etiology of nonsyndromic cleft lip with or without cleft palate (NSCL/P) in popul

261 Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a com

262 Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a com

263 Nonsyndromic cleft lip with or without cleft palate (nsCL/P) is among

264 Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one o

265 Previously we have shown that nonsyndromic cleft lip with or without cleft palate (NSCL/P) is stron

266 veral genetic risk variants for nonsyndromic cleft lip with or without cleft palate (NSCL/P).

267 P genes as candidate genes for non-syndromic cleft lip with or without cleft palate (NSCL/P).

268 Non-syndromic cleft lip with or without cleft palate (NSCLP) is a comm

269 Non-syndromic cleft lip with or without cleft palate (NSCLP) results f

270 ing) were more likely to have an infant with cleft lip with or without cleft palate (odds ratio = 2.2

271 separated into two different phenotypes: (1) cleft lip with or without cleft palate and (2) cleft pal

272 ,019 nonsyndromic orofacial cleft cases (814 cleft lip with or without cleft palate and 205 cleft pal

273 For males, the risk of cleft lip with or without cleft palate at this locus dec

274 Cleft lip with or without cleft palate is a common birth

275 Cleft lip with or without cleft palate is a common birth

276 Cleft lip with or without cleft palate is the most commo

277 rnal smoking were most elevated for isolated cleft lip with or without cleft palate, (odds ratio 2.1

278 .7), cleft palate, 0.9 (95% CI 0.5-1.6), and cleft lip with or without cleft palate, 1.3 (95% CI 0.8-

279 A total of 305 liveborn infants with cleft lip with or without cleft palate, 123 with cleft p

280 Participants were 377 infants with cleft lip with or without cleft palate, 196 with cleft p

281 Eight case groups were included: cleft lip with or without cleft palate, cleft palate onl

282 Distinguishing characteristics include cleft lip with or without cleft palate, isolated cleft p

283 common birth defects, including hypospadias, cleft lip with or without cleft palate, or hydrocephalus

284 toward understanding the genetic etiology of cleft lip with or without cleft palate, relatively littl

285 d into two groups, isolated cleft palate and cleft lip with or without cleft palate, representing a h

286 ng causal genes for isolated or nonsyndromic cleft lip with or without cleft palate.

287 f maxillofacial growth in patients born with cleft lip with or without cleft palate.

288 ion analyses for cleft palate only (CPO) and cleft lip with or without palate (CL/P) with ~17 million

289 Cleft lip with or without palate (CLP) and isolated clef

290 Our sample included 814 non-syndromic cleft lip with or without palate (NSCL/P), 205 non-syndr

291 Non-syndromic cleft lip with palate (NSCLP) is the most serious sub-ph

292 ndromic cleft lip only (NSCLO), nonsyndromic cleft lip with palate (NSCLP), and nonsyndromic cleft pa

293 alysis, cleft lip with/without cleft palate, cleft lip with palate plus cleft palate only, and all da

294 The etiology of cleft lip with/without cleft palate (CL/P), one of the m

295 Nonsyndromic cleft lip with/without cleft palate (nsCL/P) and nonsynd

296 h transmission disequilibrium test analysis, cleft lip with/without cleft palate, cleft lip with pala

297 focused on subtypes other than non-syndromic cleft lip with/without cleft palate, or investigated sub

298 P1 (combined clefts), ARHGEF18 and ARHGEF19 (cleft lip with/without palate), FBN2 (cleft lip only), S

299 Cleft lip, with or without cleft palate (CL/P), is one o

300 sociated with IRF6 are major contributors to cleft lip, with or without cleft palate.