(Q52610871)

4 May 2018

title

Anatomic and etiological classification of congenital limb deficiencies. (English)

1 reference

4 May 2018

author name string

Nina B Gold

series ordinal

1

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4 May 2018

Marie-Noel Westgate

series ordinal

2

1 reference

4 May 2018

Lewis B Holmes

series ordinal

3

1 reference

4 May 2018

language of work or name

English

0 references

publication date

9 May 2011

1 reference

4 May 2018

American Journal of Medical Genetics

published in

1 reference

4 May 2018

volume

155A

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4 May 2018

page(s)

1225-1235

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4 May 2018

issue

6

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4 May 2018

Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Unilateral transverse arm defect with subterminal digital nubbins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Academicians are more likely to share each other's toothbrush than each other's nomenclature [Cohen, 1982]

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Maternal factors, medications, and drug exposure in congenital limb reduction defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3–13.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Chorionic villus sampling: a distinctive teratogenic effect on fingers?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Hypoplasia of the second metacarpal in mother and daughter

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies: an autosomal recessive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

21 January 2018

The Holt-Oram syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Limb deficiencies in newborn infants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Unilateral terminal aphalangia in father and daughter--exogenous or genetic cause?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Trends in congenital malformations, 1974-1999: effect of prenatal diagnosis and elective termination

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Defects and Disabilities of Thalidomide Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

A classification for congenital limb malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

Point mutations in human GLI3 cause Greig syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.33999

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.33999

1 reference

4 May 2018

release_dsw55zk6x5bsljii2d5mtzjdzq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dsw55zk6x5bsljii2d5mtzjdzq

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

21557466

1 reference

4 May 2018