A locus for brachydactyly type A-1 maps to chromosome 2q35-q36. (Q34145418)

31 July 2017

title

A locus for brachydactyly type A-1 maps to chromosome 2q35-q36. (English)

1 reference

31 July 2017

Yang X

1

1 reference

31 July 2017

She C

2

1 reference

31 July 2017

Guo J

3

1 reference

31 July 2017

Yu AC

4

1 reference

31 July 2017

Lu Y

5

1 reference

31 July 2017

Shi X

6

1 reference

31 July 2017

Feng G

7

1 reference

31 July 2017

He L

8

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31 July 2017

language of work or name

English

0 references

publication date

1 March 2000

1 reference

American Journal of Human Genetics

31 July 2017

published in

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31 July 2017

volume

66

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31 July 2017

issue

3

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31 July 2017

page(s)

892-903

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

31 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=1288170

Mutations in CDMP1 cause autosomal dominant brachydactyly type C

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

A comprehensive genetic map of the human genome based on 5,264 microsatellites

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

The mutational spectrum in Waardenburg syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

Easy calculations of lod scores and genetic risks on small computers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

Classification and identification of inherited brachydactylies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288170

A boy with severe manifestations of type A1 brachydactyly

5 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10712204

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Regular dominance of thumb ankylosis with mental retardation transmitted over 3 generations]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10712204

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/302806

1 reference

31 July 2017

1 reference

31 July 2017

1 reference