'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.-Reference-Cited by-同舟云学术

'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.

Published:1977-08-01 Issue:4 Volume:14 Page:271-274
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Brimblecombe F S,Lewis F J,Vowles M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Presumptive trisomy of the short arm of B5 chromosome;Brimblecombe, F.S.W.; Lewis, F.J.W.;Human Chromosome Newsletter,1966

2. A family with an inherited translocation involving the No. 4/No. 21 chromosomes;Darmady, J.H.; Seabright, M.A.;Journal ofMedical Genetics,1975

3. Translocation heterozygosis: a cause of five cases of cri-du-chat syndrome and two cases with a duplication of chromosome number 5 in three families;American Journal of Human Genetics,1967

4. A 4-5/21-22 chromosomal translocation associated with multiple congenital anomalies;Gustavson, K.H.; Finley, S.C.; Finley, W.H.; Jalling, B.;Acta Paediatrica,1964

5. Etude genetique et clinique d'une famille de sept enfants dans laquelle trois sujets son atteints de la 'maladie due cri-du-chat';Laurent, D.; M, Robert J.;Annals de GCenetique,1966

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