Greig syndrome in a large kindred due to reciprocal chromosome translocation t(6;7)(q27;p13)
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1Children's University Hospital, Wilhelm Pieck University, Rostock, German Democratic Republic.
American Journal of Medical Genetics
|March 1, 1989
Abstract:
We report on cases of Greig syndrome segregating in a large kindred over four generations due to reciprocal translocation t(6;7)(q27;p13) and on a patient from this pedigree with a severe malformation syndrome due to duplication 7(p13----pter). The clinical findings are discussed as possible consequence of a gene mutation due to the break at 7p13.