Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region-Reference-Cited by-同舟云学术

Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region

Published:2009-01-27 Issue:8 Volume:18 Page:1377-1383
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Coppinger J.,McDonald-McGinn D.,Zackai E.,Shane K.,Atkin J. F.,Asamoah A.,Leland R.,Weaver D. D.,Lansky-Shafer S.,Schmidt K.,Feldman H.,Cohen W.,Phalin J.,Powell B.,Ballif B. C.,Theisen A.,Geiger E.,Haldeman-Englert C.,Shaikh T. H.,Saitta S.,Bejjani B. A.,Shaffer L. G.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/18/8/1377/1566603/ddp042.pdf

Reference32 articles.

1. Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

2. A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

3. 22q11.2 duplication syndrome: Two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes

4. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

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