Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.

Teh, B T

Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas. [electronic resource] - The Journal of clinical endocrinology and metabolism Dec 1996 - 4204-11 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0021-972X

10.1210/jcem.81.12.8954016 doi


Adult
Aged
Chromosome Deletion
Chromosomes, Human, Pair 1
Female
Genetic Linkage
Hamartoma--genetics
Humans
Hyperparathyroidism--genetics
Jaw Neoplasms--genetics
Kidney Diseases--genetics
Kidney Diseases, Cystic--genetics
Male