Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases-Reference-Cited by-同舟云学术

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases

Published:1984-07 Issue:2 Volume:67 Page:219-221
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Turleau Catherine,de Grouchy Jean,Chavin-Colin Françoise,Martelli Hélène,Voyer Marcel,Charlas Robert

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00273006.pdf

Reference10 articles.

1. Beckwith JB (1963) Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas, and Leydig-cell hyperplasia: another syndrome? Western Society for Pediatric Research. Los Angeles, California, Nov. 11, 1963

2. Cohen MM Jr, Ulstrom AR (1979) Beckwith-Wiedemann syndrome. In: Bergsma D (ed) Birth defects compendium, 2nd edn. The National Foundation March of Dimes. Alan R Liss, New York

3. Falk RE, Carrel RE, Valente M, Crandall BF, Sparkes RS (1973) Partial trisomy of chromosome 11: a case report. Am J Ment Defic 77:383?388

4. Goodman RM, Gorlin RJ (1977) Atlas of the face in genetic disorders, 2nd edn. Mosby Co, St Louis, p 585

5. Human Gene Mapping VII (1984) Seventh international workshop on human gene mapping. Cytogenet Cell Genet 37:1?666

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