(Q28216571)

English

Distal 5q deletion syndrome: phenotypic correlations

scientific article (publication date: 15 September 2001)

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Europe PubMed Central

title

Distal 5q deletion syndrome: phenotypic correlations (English)

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author name string

I A Schafer

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1

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N H Robin

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2

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J J Posch

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3

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B A Clark

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4

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S Izumo

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5

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S Schwartz

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6

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language of work or name

English

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publication date

15 September 2001

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published in

American Journal of Medical Genetics Part A

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volume

103

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issue

1

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page(s)

63-8

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cites work

Transcriptional antagonism between Hmx1 and Nkx2.5 for a shared DNA-binding site

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21 January 2018

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

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21 January 2018

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21 January 2018

Distinct temporal expression of mouse Nkx-5.1 and Nkx-5.2 homeobox genes during brain and ear development

1 reference

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Crossref

reference URL

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retrieved

21 January 2018

Congenital heart disease caused by mutations in the transcription factor NKX2-5

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.1513

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21 January 2018

Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4

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https://api.crossref.org/works/10.1002%2FAJMG.1513

21 January 2018

1 reference

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21 January 2018

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

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reference URL

https://api.crossref.org/works/10.1002%2FAJMG.1513

retrieved

21 January 2018

A case of de novo interstitial deletion of chromosome 5(q33q34).

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FAJMG.1513

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21 January 2018

Ventricular noncompaction and distal chromosome 5q deletion

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21 January 2018

Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardation

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reference URL

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retrieved

21 January 2018

Identifiers

DOI

10.1002/AJMG.1513

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PubMed publication ID

11562936

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(Q28216571)

Distal 5q deletion syndrome: phenotypic correlations

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