(Q51953576)

18 April 2018

title

Interstitial microdeletion of chromosome 1p in two siblings. (English)

1 reference

18 April 2018

1 reference

Campbell CG

1

1 reference

18 April 2018

Wang H

series ordinal

2

1 reference

18 April 2018

Hunter GW

series ordinal

3

1 reference

18 April 2018

publication date

1 August 2002

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18 April 2018

American Journal of Medical Genetics Part A

published in

1 reference

18 April 2018

volume

111

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18 April 2018

issue

3

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18 April 2018

page(s)

289-294

1 reference

18 April 2018

Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10595

Uniparental isodisomy resulting from 46,XX,i(1p),i(1q) in a woman with short stature, ptosis, micro/retrognathia, myopathy, deafness, and sterility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10595

Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10595

Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10595

Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10595

21 January 2018

Identifiers

DOI

10.1002/AJMG.10595

1 reference

18 April 2018

1 reference

18 April 2018