(Q28204788)

https://api.crossref.org/works/10.1002%2FAJMG.10776

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A CASE OF “ANGEIO-KERATOMA.”

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Molecular evolution of the homeodomain family of transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Homeotic genes and the evolution of arthropods and chordates

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

21 January 2018

Fetal valproate syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A mouse model for valproate teratogenicity: parental effects, homeotic transformations, and altered HOX expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Developmental functions of mammalian Hox genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Comparison of X-ray and NMR structures for the Antennapedia homeodomain-DNA complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

21 January 2018

Exploring the homeobox

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Homeodomain-DNA recognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

21 January 2018

Human HOX gene mutations

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Drosophila Hox complex downstream targets and the function of homeotic genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

The hand-foot-genital (hand-foot-uterus) syndrome: family report and update

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Transcriptional repression by the Drosophila even-skipped protein: definition of a minimal repression domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Hox gene expression in limbs: colinearity by opposite regulatory controls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Trinucleotide repeats and long homopeptides in genes and proteins associated with nervous system disease and development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

If birds can fly, why can't we? Homeotic genes and evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Breaking colinearity in the mouse HoxD complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Of fingers, toes and penises.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Valproic acid embryopathy: report of two siblings with further expansion of the phenotypic abnormalities and a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Hox genes in vertebrate development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A gene complex controlling segmentation in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Homology modeling using simulated annealing of restrained molecular dynamics and conformational search calculations with CONGEN: application in predicting the three-dimensional structure of murine homeodomain Msx-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Mapping and mutagenesis of the amino-terminal transcriptional repression domain of the Drosophila Krüppel protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Homeobox genes in embryogenesis and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Homeobox genes and axial patterning

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Mutation of HOXA13 in hand-foot-genital syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Know your neighbors: three phenotypes in null mutants of the myogenic bHLH gene MRF4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Infertility in adult hypodactyly mice is associated with hypoplasia of distal reproductive structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Radiographic findings in the hand-foot-uterus syndrome (HFUS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Two cases with interstitial deletions of chromosome 2 and sex reversal in one.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

The hand-food-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Breakpoint analysis of a familial balanced translocation t(2;8)(q31;p21) associated with mesomelic dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Gene transpositions in the HoxD complex reveal a hierarchy of regulatory controls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Polyalanine expansion in synpolydactyly might result from unequal crossing-over of HOXD13

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

Synpolydactyly in mice with a targeted deficiency in the HoxD complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10776

21 January 2018

Identifiers

DOI

10.1002/AJMG.10776

1 reference

Consolidated OpenCitations Corpus – April 2017

1003142

1003142

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference