Interstitial deletion of the short arm of chromosome 2 in a mother and child, with facial dysmorphism and mild learning difficulties-Reference-Cited by-同舟云学术

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Interstitial deletion of the short arm of chromosome 2 in a mother and child, with facial dysmorphism and mild learning difficulties

Published:2006-10 Issue:4 Volume:15 Page:221-223
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Armstrong Ruth,Ellis Ian,Kightley Catherine,Sethi Vijay Dinanadh,McCarthy Emma,Maye Una,White Gillian

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference8 articles.

1. Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmata;Fryns;Hum Genet,1979

2. Syndromes of the head and neck. 4th ed;Gorlin,2001

3. Prenatal detection of cyclopia associated with interstitial deletion of 2p;Grundy;Am J Med Genet,1989

4. A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer;Lucci-Cordisco;Clin Genet,2004

5. Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature;Münke;Am J Med Genet,1988

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017

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