Prader-Willi syndrome and Robertsonian translocations involving chromosome 15-Reference-Cited by-同舟云学术

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Prader-Willi syndrome and Robertsonian translocations involving chromosome 15

Published:2008-06-28 Issue:4 Volume:39 Page:294-297
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Casamassima Anthony C.,Shapiro Lawrence R.,Wilmot Patrick L.,Smith Karen Berk

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03028.x/fullpdf

Reference15 articles.

1. The XX male-report of a child and an adult;Bauch;Endokrinologie,1980

2. Chromosome 15 in floppy infants;Berry;Arch. Dis. Child.,1982

3. Prader-Willi syndrome;Cassidy;Curr. Probl. Pediatr.,1984

4. New data for determining Prader-Willi syndrome recurrence risk;Cassidy;Am. J. Med. Genet.,1987

5. Syndrome de Prader-Willi et translocation 15-15;Emberger;Ann. Genet.,1977

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1. Overview of genetic testing in Prader-Willi syndrome;Expert Opinion on Orphan Drugs;2023-09-28

2. The role of genetic counseling in the infertile patient;Human Reproductive Genetics;2020

3. Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?;Prenatal Diagnosis;2019-08-19

4. Robertsonian translocations in Prader-Willi syndrome;Clinical Genetics;2008-06-28

5. Prader-Willi syndrome due to 15q11-q13 deletion in a girl with an inherited (13;14) Robertsonian translocation;American Journal of Medical Genetics;2002-08-15

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