about
Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).Regulation of number and size of digits by posterior Hox genes: A dose-dependent mechanism with potential evolutionary implicationsSynpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractThe HOXC11 homeodomain protein interacts with the lactase-phlorizin hydrolase promoter and stimulates HNF1alpha-dependent transcriptionMutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palateNovel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndromeDeletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD clusterSecond-to-fourth digit ratio predicts success among high-frequency financial tradersMutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndromeDifferential gene-expression patterns in genital fibroblasts of normal males and 46,XY females with androgen insensitivity syndrome: evidence for early programming involving the androgen receptorGroup 13 HOX proteins interact with the MH2 domain of R-Smads and modulate Smad transcriptional activation functions independent of HOX DNA-binding capability.Hypospadias and endocrine disruption: is there a connection?The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approachesA systematic review of association studies of common variants associated with idiopathic congenital talipes equinovarus (ICTEV) in humans in the past 30 yearsStructural basis for sequence specific DNA binding and protein dimerization of HOXA13Bisphenol A exposure alters developmental gene expression in the fetal rhesus macaque uterusAmegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutationHuman HOX gene mutationsComplete mutation analysis panel of the 39 human HOX genesLimb malformations and the human HOX genesHoxc13 mutant mice lack external hairRor2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndromeEmbryonic development of mouse external genitalia: insights into a unique mode of organogenesisBone developmentShared Enhancer Activity in the Limbs and Phallus and Functional Divergence of a Limb-Genital cis-Regulatory Element in SnakesExpanded HOXA13 polyalanine tracts in a monotremeFossils, genes and the evolution of animal limbsHuman 2D (index) and 4D (ring) finger lengths and ratios: cross-sectional data on linear growth patterns, sexual dimorphism and lateral asymmetry from 4 to 60 years of age.Comparative phylogenomic analyses of teleost fish Hox gene clusters: lessons from the cichlid fish Astatotilapia burtoni.Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndrome.Reconstructing the history of human limb development: lessons from birth defects.Mesenchymal-epithelial interactions during digestive tract development and epithelial stem cell regenerationTranscription factors in dysmorphology.Candidate gene analysis in a case of congenital absence of the endometrium.Tibial agenesis, femoral duplication, and caudal midline anomalies.Uterine disorders and pregnancy complications: insights from mouse modelsExpression pattern of the class I homeobox genes in ovarian carcinoma.Genetics of the female reproductive ducts.The effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosis
P2860
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P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Mutation of HOXA13 in hand-foot-genital syndrome
@ast
Mutation of HOXA13 in hand-foot-genital syndrome
@en
Mutation of HOXA13 in hand-foot-genital syndrome
@en-gb
Mutation of HOXA13 in hand-foot-genital syndrome
@nl
type
label
Mutation of HOXA13 in hand-foot-genital syndrome
@ast
Mutation of HOXA13 in hand-foot-genital syndrome
@en
Mutation of HOXA13 in hand-foot-genital syndrome
@en-gb
Mutation of HOXA13 in hand-foot-genital syndrome
@nl
prefLabel
Mutation of HOXA13 in hand-foot-genital syndrome
@ast
Mutation of HOXA13 in hand-foot-genital syndrome
@en
Mutation of HOXA13 in hand-foot-genital syndrome
@en-gb
Mutation of HOXA13 in hand-foot-genital syndrome
@nl
P3181
P356
P1433
P1476
Mutation of HOXA13 in hand-foot-genital syndrome
@en
P2093
D P Mortlock
P2888
P304
P3181
P356
10.1038/NG0297-179
P407
P577
1997-02-01T00:00:00Z
P6179
1045746224