(Q33498923)

27 July 2017

Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11? (English)

1 reference

autoimmune thrombocytopenic purpura

27 July 2017

0 references

1 reference

Lévy A

1

1 reference

27 July 2017

Michel G

series ordinal

2

1 reference

27 July 2017

Lemerrer M

series ordinal

3

1 reference

27 July 2017

Philip N

series ordinal

4

1 reference

27 July 2017

1 April 1997

1 reference

American Journal of Medical Genetics Part A

27 July 2017

1 reference

27 July 2017

69

1 reference

27 July 2017

356-359

1 reference

27 July 2017

4

1 reference

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

27 July 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970414%2969%3A4%3C356%3A%3AAID-AJMG4%3E3.0.CO%3B2-J

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970414%2969%3A4%3C356%3A%3AAID-AJMG4%3E3.0.CO%3B2-J

Soluble FcϵR II levels in normal children and patients with immunodeficiency diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970414%2969%3A4%3C356%3A%3AAID-AJMG4%3E3.0.CO%3B2-J

"CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970414%2969%3A4%3C356%3A%3AAID-AJMG4%3E3.0.CO%3B2-J

DiGeorge syndrome: part of CATCH 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970414%2969%3A4%3C356%3A%3AAID-AJMG4%3E3.0.CO%3B2-J

10.1002/(SICI)1096-8628(19970414)69:4<356::AID-AJMG4>3.0.CO;2-J

21 January 2018

Identifiers

DOI

1 reference

27 July 2017

1 reference