Further phenotype description, genotype characterization in patients with de novo interstitial deletion on 2p23.2-24.1-Reference-Cited by-同舟云学术

Further phenotype description, genotype characterization in patients with de novo interstitial deletion on 2p23.2-24.1

Published:2014-04-03 Issue:7 Volume:164 Page:1789-1794
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bloch Mercedes¹,Leonard Anissa²,Diplas Andreas A.¹,Pepermans Xavier¹,Emanuel Beverly S.³,Rocca Maria Santa⁴,Revencu Nicole¹,Sznajer Yves¹

Affiliation:

1. Center for Human Genetics; Cliniques Universitaires St. Luc; Université Catholique de Louvain; Brussels Belgium

2. Pediatric Department; Cliniques Universitaires St. Luc; Université Catholique de Louvain; Brussels Belgium

3. Division of Human Genetics and Department of Pediatrics; The Children's Hospital of Philadelphia; Perelman School of Medicine at the University of Pennsylvania; Philadelphia Pennsylvania

4. Institute for Maternal and Child Health IRCCS “B Garofolo”; Trieste Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36516/fullpdf

Reference11 articles.

1. Familial syndromic esophageal atresia maps to 2p23-p24;Celli;Am J Hum Genet,2000

2. Deletion mapping: Further evidence for the location of acid phosphatase (ACP1) within 2p23;Emanuel;Am J Med Genet,1979

3. An apparent de novo terminal deletion of chromosome 2 (pter-p24);Francis;J Med Genet,1990

4. Deletion of 2p: A cytogenetic and clinical update;Neidich;Am J Med Genet,1987

5. Interstitial deletion of chromosome 2 (p23p25);Penchaszadeh;Am J Med Genet,1987

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