(Q51958408)

English

Concurrent microdeletion and duplication of 22q11.2.

scientific article published on 28 April 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

Concurrent microdeletion and duplication of 22q11.2. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

Kristina Lagerstedt Robinson

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K Lagerstedt

2

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author name string

E Blennow

1

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

H Malmgren

3

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

S Sahlén

4

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

J Schoumans

5

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

Bm Anderlid

6

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

publication date

28 April 2008

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Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

Clinical Genetics

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Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

74

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Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

1

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

61-67

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01008.X

21 January 2018

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01008.X

21 January 2018

Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01008.X

21 January 2018

Identifiers

10.1111/J.1399-0004.2008.01008.X

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18445048

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