A case of 48,XXY,21+ in an infant with Down's syndrome.-Reference-Cited by-同舟云学术

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A case of 48,XXY,21+ in an infant with Down's syndrome.

Published:1971-12-01 Issue:4 Volume:8 Page:533-535
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Neu R L,Scheuer A Q,Gardner L I

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference6 articles.

1. Testicular agenesis in a boy with XY/XYY mosaicism;Carakushansky, G.; Neu, R.L.; Gardner, L.I.;Annales de Genetique,1969

2. Identification of human chromosomes by DNA-binding fluorescent agents;Caspersson, T.; Zech, L.; Johansson, C.; Modest, E.J.;Chromosoma,1970

3. Technique for identifying Y chromosomes in human interphase nuclei;Pearson, P.L.; Bobrow, M.; Vosa, C.G.;Nature,1970

4. Uchida, I. A., Ray, M., and Duncan, B. P. (1966).

5. Trisomy with an XYY sex chromosome complement;Journal of Pediatrics

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Double Trisomy 48,XXY,+21 in a Neonate with Congenital Heart Disease;Archives of Iranian Medicine;2020-05-01

2. Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes;American Journal of Medical Genetics Part A;2005

3. Double trisomy;American Journal of Medical Genetics;2003

4. Trisomy 21 with XYY;The Indian Journal of Pediatrics;2002-11

5. Another case of prenatally diagnosed 48,XYY,+21;American Journal of Medical Genetics;1995-02-13

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