scholarly journals 47,XYY syndrome

2020 ◽  
Author(s):  
Keyword(s):  
2015 ◽  
Vol 35 (5) ◽  
pp. 544-547 ◽  
Author(s):  
Ju-Heon Park ◽  
Hyun-Woo Choi ◽  
Bo-Young Seo ◽  
Min-Goo Kang ◽  
Soo-Hyun Kim ◽  
...  

PEDIATRICS ◽  
1970 ◽  
Vol 46 (3) ◽  
pp. 489-489
Author(s):  
Park S. Gerald

If you are a medical student, house officer, or practicing physician, unversed in human genetics but wanting a quick orientation, then this may be the book for you. It is brief, inexpensive, and gratifyingly up-to-date. In the 5 years since the first edition of this small book, there have been many important developments in human genetics—the use of hybrid cells for genetic analysis, the discovery of multiple structural genes for the Y chain of Hgb F, appreciation of the frequency of the XYY syndrome, the use of amniocentesis for antenatal diagnosis, and so forth.


1970 ◽  
Vol 15 (4) ◽  
pp. 389-398 ◽  
Author(s):  
Anthony M. Marcus ◽  
G. Richmond
Keyword(s):  

2008 ◽  
Vol 5 (5) ◽  
pp. 387-394 ◽  
Author(s):  
B. Noël ◽  
J. P. Duport ◽  
D. Revil ◽  
I. Dussuyer ◽  
B. Quack
Keyword(s):  

2000 ◽  
Vol 30 (2) ◽  
pp. 91-95 ◽  
Author(s):  
Nkanginieme Ike

1974 ◽  
Vol 125 (586) ◽  
pp. 236-237 ◽  
Author(s):  
Johannes Nielsen ◽  
Takayuki Tsuboi

Previous electroencephalographic studies of persons with sex chromosome aberrations have indicated that there might be more electroencephalographic aberrations in males with double Y and double X than in the general population. A survey of these studies has recently been made by Fenton et al. (1971).


2019 ◽  
Vol 32 (2) ◽  
pp. 87-94 ◽  
Author(s):  
Francesca F. Operto ◽  
Grazia M.G. Pastorino ◽  
Elisabetta Amadori ◽  
Roberta Mazza ◽  
Pia Bernardo ◽  
...  

2008 ◽  
Vol 3 (3) ◽  
pp. 162-168 ◽  
Author(s):  
M. T. Alam ◽  
R. Deschamps ◽  
E. Gaba ◽  
S. S. Kasatiya ◽  
W. F. Grant

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