(Q41725573)

8 October 2017

1 reference

title

Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance (English)

1 reference

8 October 2017

1 reference

Pinto-Escalante D

1

1 reference

8 October 2017

Ceballos-Quintal JM

series ordinal

2

1 reference

8 October 2017

Castillo-Zapata I

series ordinal

3

1 reference

8 October 2017

Canto-Herrera J

series ordinal

4

1 reference

8 October 2017

publication date

1 March 1998

1 reference

American Journal of Medical Genetics Part A

8 October 2017

published in

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8 October 2017

volume

76

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8 October 2017

issue

2

1 reference

8 October 2017

page(s)

150-153

1 reference

Monosomy of chromosome No. 22. A case report.

8 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980305%2976%3A2%3C150%3A%3AAID-AJMG8%3E3.0.CO%3B2-X

Crossref

reference URL

Excess of deletions of maternal origin in the DiGeorge/Velo-cardio-facial syndromes. A study of 22 new patients and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980305%2976%3A2%3C150%3A%3AAID-AJMG8%3E3.0.CO%3B2-X

Crossref

reference URL

10.1002/(SICI)1096-8628(19980305)76:2<150::AID-AJMG8>3.0.CO;2-X

21 January 2018

Identifiers

DOI

1 reference

8 October 2017

1 reference