1.
Article
in English
| IMSEAR
| ID: sea-16507
ABSTRACT
Polymerase chain reaction (PCR) was used to study the presence of gene deletion (the most prominent type of mutations) in some families afflicted by Duchenne muscular dystrophy/Becker muscular dystrophy (DMD/BMD). The results clearly demonstrate deletion in the central part of the DMD gene in two of the three families studied. This information can be useful for genetic counselling with particular reference to prenatal diagnosis and carrier analysis.
Subject(s)
Base Sequence , Gene Deletion , Humans , Molecular Sequence Data , Muscular Dystrophies/blood , Polymerase Chain Reaction
2.
Article
in English
| IMSEAR
| ID: sea-26140
3.
Medicina (B.Aires)
;
46(4): 476-7, jul.-ago. 1986. tab
Article
in Spanish
| LILACS
| ID: lil-41987
4.
Article
in English
| IMSEAR
| ID: sea-16150
5.
Indian J Med Sci
;
1967 Jan; 21(1): 38-43
Article
in English
| IMSEAR
| ID: sea-67182
Subject(s)
Adolescent , Adult , Central Nervous System Diseases/blood , Child , Child, Preschool , Female , Fructose-Bisphosphate Aldolase/blood , Humans , Infant , Male , Middle Aged , Muscular Dystrophies/blood
6.
Neurol India
;
1966 Oct-Dec; 14(4): 167-73
Article
in English
| IMSEAR
| ID: sea-121777