DISEASE
|
CHROMOSOME/GENE INVOLVED
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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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