(Q52547883)

3 May 2018

title

Mutational analysis of HOXD13 and HOXA13 genes in the triphalangeal thumb-brachyectrodactyly syndrome. (English)

1 reference

3 May 2018

1 reference

Pérez-Cabrera A

1

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3 May 2018

Kofman-Alfaro S

series ordinal

2

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3 May 2018

Zenteno JC

series ordinal

3

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3 May 2018

publication date

1 September 2002

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3 May 2018

Journal of Orthopaedic Research

published in

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3 May 2018

volume

20

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3 May 2018

issue

5

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3 May 2018

page(s)

899-901

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3 May 2018

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

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/10.1016%2FS0736-0266%2802%2900008-6

Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Molecular analysis of SALL1 mutations in Townes-Brocks syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Genetics of limb anomalies in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Mutation of HOXA13 in hand-foot-genital syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

The sonic hedgehog-patched-gli pathway in human development and disease

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Hox genes in digit development and evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Regulation of number and size of digits by posterior Hox genes: A dose-dependent mechanism with potential evolutionary implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

A new syndrome of triphalangeal thumbs and brachy-ectrodactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Triphalangeal thumbs‐ectrodactyly in a sporadic case

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Triphalangeal thumb and brachyectrodactyly syndrome: an uncommon entity with evidence of geographic distribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0736-0266%2802%2900008-6

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0736-0266(02)00008-6

1 reference

3 May 2018

PubMed ID

12382951

1 reference

3 May 2018