Genetic counseling in Becker type X-linked muscular dystrophy. I. Theoretical considerations

1984 ◽  
Vol 18 (4) ◽  
pp. 713-718 ◽  
Author(s):  
T. Grimm ◽  
John M. Opitz ◽  
James F. Reynolds
1997 ◽  
Vol 7 (6-7) ◽  
pp. 434
Author(s):  
Cyril Legum ◽  
Avi Orr-Urtreger ◽  
Adi Ben Yehuda ◽  
Chedva Perek ◽  
Sigal Tsabari ◽  
...  

1977 ◽  
Vol 23 (12) ◽  
pp. 2341-2343 ◽  
Author(s):  
H L Verrill ◽  
N A Pickard ◽  
H D Gruemer

Abstract Currently, the most useful clinical laboratory aid in establishing the carrier state of Duchenne muscular dystrophy is to determine creatine kinase (EC 2.7.3.2) activity in the plasma. The considerable overlap between plasma creatine kinase activities of controls and of carriers at the childbearing age contributes appreciable difficulty to genetic counseling of potential carriers. The consistent failure of lymphocyte cap formation in Duchenne muscular dystrophy patients and carriers in this study suggests a valuable tool for the confirmation of the carrier state.


1995 ◽  
Vol 18 (S13) ◽  
pp. S103-S109 ◽  
Author(s):  
Peter W. Lunt ◽  
Philip E. Jardine ◽  
Manuela Koch ◽  
Julia Maynard ◽  
Micheal Osborn ◽  
...  

2011 ◽  
Vol 21 (4) ◽  
pp. 557-563 ◽  
Author(s):  
Miri Yanoov-Sharav ◽  
Esther Leshinsky-Silver ◽  
Sarit Cohen ◽  
Chana Vinkler ◽  
Marina Michelson ◽  
...  

1999 ◽  
Vol 55 (5) ◽  
pp. 377-381 ◽  
Author(s):  
Ma Alcántara ◽  
Mt Villarreal ◽  
V Del Castillo ◽  
G Gutiérrez ◽  
Y Saldaña ◽  
...  

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