Double chromosome anomaly: Interstitial deletion 5q and reciprocal translocation (1;11) (p22;q21)-Reference-Cited by-同舟云学术

Double chromosome anomaly: Interstitial deletion 5q and reciprocal translocation (1;11) (p22;q21)

Published:1990-05 Issue:1 Volume:36 Page:29-32
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

de Michelena María I.,Villacorta Jorge,Chávez Julio

Publisher

Wiley

Subject

Genetics(clinical)

Reference10 articles.

1. Localization of the gene for familial adenomatous polyposis on chromosome 5

2. A child with interstitial deletion of chromosome No. 5

3. Gardner syndrome in a man with an interstitial deletion of 5q

4. Deletion of chromosome 5q and familial adenomatous polyposis.

5. (1978): 46, XX, del(5)(pter to q15::q23 to qter). In (eds): “Repository of Chromosomal Variants and Anomalies in Man,” Ed 5. Denton: North Texas University; p 56.

Cited by 11 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. Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes;American Journal of Medical Genetics Part A;2011-07-08

2. Alpha-1 Antitrypsin Genotypes in Breast Cancer Patients;Journal of Health Science;2008

3. Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature;Prenatal Diagnosis;2006

4. Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences;American Journal of Medical Genetics Part A;2006

5. Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene;Journal of Human Genetics;2005-12-20