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[Detection of dystrophin gene mutation carrier state]
M Bisko1, J G Zimowski, E Fidziańska
1Zakładu Genetyki, Instytutu Psychiatrii i Neurologii w Warszawie.
Neurologia I Neurochirurgia Polska
|March 1, 1996
Abstract:
RFLP polymorphism and the sequence of repeated CA were analysed by means of polymerase chain reaction in 62 families in which cases of DMD/BMD had occurred. The established carriers were suggested to undergo prenatal examinations for avoiding giving birth to a child with Duchenne or Becker type of muscular dystrophy.