(Q52088295)

English

X-chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred.

scientific article published in February 1987

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

X-chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred. (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

1 reference

based on heuristic

inferred from title

author name string

M Ahmad

1

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

H Abbas

2

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

S Haque

3

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

G Flatz

4

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

publication date

1 February 1987

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

75

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

2

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

169-173

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

https://scigraph.springernature.com/pub.10.1007/bf00591081

0 references

[Delayed mutation in man; a critical observation on the work of Ch. Auerbachs (1956)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3817811

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Recessive Form of Ectrodactyly, and its Implications in Genetic Counseling

1 reference

https://pubmed.ncbi.nlm.nih.gov/3817811

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial occurrence of severe ulnar aplasia and lobster claw feet: A new syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3817811

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monodactylous splithand-splitfoot. A malformation occurring in three distinct genetic types

1 reference

https://pubmed.ncbi.nlm.nih.gov/3817811

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00591081

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/3817811

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q52088295&oldid=1702397895"