Partial trisomy 1, karyotype 46,XY,12-,t(1q, 12p)+-Reference-Cited by-同舟云学术

Partial trisomy 1, karyotype 46,XY,12-,t(1q, 12p)+

Published:1973 Issue:3 Volume:18 Page:225-230
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Berghe H.,Eygen M.,Fryns J. P.,Tanghe W.,Verresen H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00290601.pdf

Reference20 articles.

1. Aarskog, D.: A large deletion of chromosome n0 1 (45,XY,1?..). J. med. Genet. 5, 322?325 (1968).

2. Boué, J. G., Boué, A.: Fréquence des aberrations chromosomiques dans les avortements spontanés humains. C. R. Acad. Sc. (Paris) 269, 283?286 (1969).

3. Collett, R. W., Edwards, J. E.: Persistent truncus arteriosus; classification according to anatomic types. Surg.Clin. N. Amer. 29, 1245?1270 (1949).

4. Cooper, H. L., Hernits, R.: Familial chromosome variant in a subject with anomalous sex differentiation. Amer. J. hum. Genet. 15, 465?475 (1963).

5. De Grouchy, J., Lautmann, F.: 46,XX,1q-,2q-,Dq+,16q+ in a polymalformed child. Ann. Génét. 11, 129?131 (1968).

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