A girl with the Prader-Willi Syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members-Reference-Cited by-同舟云学术

A girl with the Prader-Willi Syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members

Published:1980-08 Issue:2 Volume:55 Page:271-273
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Smith Arabella,Noel Michael

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00291777.pdf

Reference24 articles.

1. Arrighi FE, Hsu TC (1971) Localisation of heterochromatin in human chromosomes. Cytogenet Cell Genet 10:81?86

2. Carrel RE, Sparkes RS, Wright SW (1973). Chromosome survey of moderately to profoundly retarded patients. Am J Ment Defic 77:616?622

3. Cohen MM (1971) The chromosomal constitution of 165 human translocations involving D group chromosomes identified by auto-radiography. Ann Genet (Paris) 14:87?96

4. Doyle CT (1976) The cytogenetics of 90 patients with idiopathic mental retardation malformation syndromes and of 90 normal subjects. Hum Genet 33:131?146

5. Emberger JM, Rodiere M, Astruc J, Brunel D (1977) Syndrome de Prader-Willi et translocation 15?15. Ann Genet (Paris) 20:297?300

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