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SQUMJ-Sultan Qaboos University Medical Journal. 2013; 13 (2): 311-317
in English | IMEMR | ID: emr-126037

ABSTRACT

Female carriers of balanced translocations involving an X chromosome and an autosome present genetic councelling challenges. This is in view of the number of possible meiotic outcomes, but also due to the impact of X chromosome-localised genes that are no longer subject to gene silencing through the X chromosome inactivation centre. We present a case where delineation of the extent of X chromosome-localised genes on the derivative autosome using molecular karyotyping offers critical information in the context of genetic councelling


Subject(s)
Humans , Male , Developmental Disabilities , Genetic Counseling , Chromosomes, Human, X , Patient Outcome Assessment , Nerve Tissue Proteins , Translocation, Genetic
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