Duplication deficiency syndrome in familial translocation (2q-; 5p+)-Reference-Cited by-同舟云学术

Duplication deficiency syndrome in familial translocation (2q-; 5p+)

Published:1971 Issue:2 Volume:12 Page:110-122
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Bijlsma J. B.,France H.,Bleeker-Wagemakers E. M.,Wijefels J. C. H. M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00291466.pdf

Reference14 articles.

1. Edwards, J. H., Fraccaro, M., Davies, P., Young, R. B.: Structural heterozygosis in man: analysis of two families. Ann. hum. Genet. 26, 163?178 (1962).

2. Gey, W.: Untersuchungen �ber die DNS-Replikationsumster der Chromosomengruppe 4?5, 13?15 und 21?22 an in vitro gez�chteten menschlichen Lymphocyten. Humangenetik 2, 246?261 (1966).

3. de, Grouchy, J.: Complex familial chromosome translocation. Amer. J. hum. Genet. 17, 501?509 (1965).

4. Hamerton, J. O.: Reciprocal translocations in man. Chromosomes today. 2, 21?32 (1969).

5. Harnden, D. G.: A human skin culture technique used for cytological examinations. Brit. J. exp. Path. 49, 31?37 (1960).

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