Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13.
主要な著者: | Cianferotti, L, Pannett, A, Whyte, M, Thakker, R |
---|---|
フォーマット: | Journal article |
出版事項: |
1999
|
類似資料
-
LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
著者:: Trump, D, 等
出版事項: (1995) -
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.
著者:: Lloyd, SE, 等
出版事項: (1999) -
Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.
著者:: Trump, D, 等
出版事項: (1995) -
Familial benign hypercalcaemia, Oklahoma variant (FBHok): Localisation to chromosome 19q13.
著者:: Lloyd, SE, 等
出版事項: (1997) -
Identification of a second kindred with familial hypocalciuric hypercalcemia type 3 (FHH3) narrows localization to a <3.5 megabase pair region on chromosome 19q13.3.
著者:: Nesbit, M, 等
出版事項: (2010)