Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: Two patients and review of the literature-Reference-Cited by-同舟云学术

Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: Two patients and review of the literature

Published:2007 Issue:18 Volume:143A Page:2204-2212
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Klaassens M.,Galjaard R.J.H.,Scott D.A.,Brüggenwirth H.T.,van Opstal D.,Fox M.V.,Higgins R.R.,Cohen-Overbeek T.E.,Schoonderwaldt E.M.,Lee B.,Tibboel D.,de Klein A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference37 articles.

1. Congenital diaphragmatic hernia in a family segregating a reciprocal translocation t(5;15)(p15.3;q24)

2. Two cases of prenatally diagnosed diaphragmatic hernia accompanied by the same undescribed chromosomal deletion (15q24 de novo)

3. Congenital diaphragmatic hernia: Is 15q26.1-26.2 a candidate locus?

4. Narrowing the Candidate Region for Congenital Diaphragmatic Hernia in Chromosome 15q26: Contradictory Results

5. Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, uinary tract anomalies, congenital heart defect and kyphoscoliosis

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