X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.-Reference-Cited by-同舟云学术

X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.

Published:1979-08-01 Issue:4 Volume:16 Page:254-262
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Bernstein R,Dawson B,Kohl R,Jenkins T

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference31 articles.

1. Karyotyp-Phenotyp-Korrelation bei einem 46, X del (X) (p. 22) Befund;Bartsch-Sandhoff, M.; Terinde, R.; Wiegelmann, W.; Scholz, W.;Human Genetics,1976

2. Repository of Chromosomal Variants and Anomalies in Man. Fourth Listing;Borgaonkar, D.S.; Dolling, D.R.,1977

3. Genetic variation of the soluble form of NADP dependent isocitrate dehydrogenase;Chen, S.-H.; Fossum, B.L.G.; Giblett, E.R.;American Journal of Human Genetics,1972

4. Polymorphism of soluble glutamic-pyruvate transaminase: a new genetic marker in man;Chen, S.-H.; Giblett, E.R.;Science,1971

5. Two human X-autosome translocations identified by autoradiography and fluorescence;Cohen, M.M.; Lin, C.-C.; Sybert, V.; Orecchio, E.J.;American Journal of Human Genetics,1972

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