del(15)(q22q24) Syndrome with Potter sequence-Reference-Cited by-同舟云学术

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del(15)(q22q24) Syndrome with Potter sequence

Published:1984-12 Issue:4 Volume:19 Page:703-705
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Clark Robin Dawn

Publisher

Wiley

Subject

Genetics (clinical)

Reference1 articles.

1. (1984): The Potter sequence: A clinical analysis of 80 cases. Am J Med Genet, this issue.

Cited by 22 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. CHD2-Related CNS Pathologies;International Journal of Molecular Sciences;2021-01-08

2. Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review;Molecular Genetics & Genomic Medicine;2020-05-13

3. De novointerstitial deletion of 15q22q23 with global developmental delay and hypotonia: the first Korean case;Korean Journal of Pediatrics;2015

4. Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping;Human Genetics;2009-06-26

5. Genetic syndromes and prenatally detected renal anomalies;Seminars in Fetal and Neonatal Medicine;2008-06

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