(Q33909995)

30 July 2017

0 references

A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease (English)

1 reference

30 July 2017

0 references

Antonio M Persico

7

0 references

Frank A Middleton

6

object named as

Frank A Middleton

1 reference

30 July 2017

Antony E Shrimpton

1

1 reference

30 July 2017

E Mark Levinsohn

2

1 reference

30 July 2017

Justin M Yozawitz

3

1 reference

30 July 2017

David S Packard

4

1 reference

30 July 2017

Robert B Cady

5

1 reference

30 July 2017

David R Hootnick

8

1 reference

30 July 2017

language of work or name

English

0 references

publication date

14 May 2004

1 reference

American Journal of Human Genetics

30 July 2017

published in

1 reference

30 July 2017

volume

75

1 reference

30 July 2017

issue

1

1 reference

30 July 2017

page(s)

92-96

1 reference

Limb malformations and the human HOX genes

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Autosomal dominant transmission of isolated congenital vertical talus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

28 July 2018

Human HOX gene mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Mutation of HOXA13 in hand-foot-genital syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Analysis of Hox gene expression in the chick limb bud.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Differential DNA-binding specificity of the engrailed homeodomain: the role of residue 50.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

The degree of variation in DNA sequence recognition among four Drosophila homeotic proteins.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Hox genes in vertebrate development

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

A Genetic Model for Interaction of the Homeodomain Recognition Helix with DNA

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Congenital vertical talus and its familial occurrence: an analysis of 36 patients

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Large-scale genotyping of complex DNA.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182012

Making progress with limb models

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15146389

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Congenital vertical talus: classification with 69 cases and new measurement system

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15146389

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Autosomal dominant transmission of isolated congenital vertical talus

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15146389

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/422015

1 reference

30 July 2017

1 reference

30 July 2017

1 reference