Sunday, May 19, 2013

DISEASE/CHROMOSOME


DISEASE
CHROMOSOME/GENE INVOLVED
SCHIZOPHRENIA
DELETION AT 15q and 1q
AUTISM
DELETION AT 15q and 16p
EPILEPSY
16p DELETION
AUTISM
DUPLICATION OF X LINKED MeCP2 GENE
RETT SYNDROME
POINT MUTATION OF MeCP2 GENE


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