Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within thePWCR-Reference-Cited by-同舟云学术

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Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within thePWCR

Published:1990-04 Issue:4 Volume:35 Page:536-545
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gregory C. A.,Kirkilionis A. J.,Greenberg C. R.,Chudley A. E.,Hamerton J. L.

Publisher

Wiley

Subject

Genetics(clinical)

Reference32 articles.

1. PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROME

2. Publisher's note

4. Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.

Cited by 27 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. Tentative classification of neuropsychiatric disturbances in Parader-Willi syndrome;Journal of Intellectual Disability Research;2008-06-28

2. Differentiated recurrence risk estimations in the Prader-Willi syndrome;Clinical Genetics;2008-06-28

3. Salivary Abnormalities in Prader-Willi Syndrome;Annals of the New York Academy of Sciences;1998-04

4. A case of Prader-Willi syndrome associated with mosaicism: Cytogenetic and FISH study.;Genes & Genetic Systems;1996

5. A variety of genetic mechanisms are associated with the Prader-Willi syndrome;American Journal of Medical Genetics;1994-09-15

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