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Genetic mapping studies of fam...
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Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13.
Bibliografiska uppgifter
Huvudupphovsmän:
Cianferotti, L
,
Pannett, A
,
Whyte, M
,
Thakker, R
Materialtyp:
Journal article
Publicerad:
1999
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Liknande verk
LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
av: Trump, D, et al.
Publicerad: (1995)
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.
av: Lloyd, SE, et al.
Publicerad: (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.
av: Trump, D, et al.
Publicerad: (1995)
Familial benign hypercalcaemia, Oklahoma variant (FBHok): Localisation to chromosome 19q13.
av: Lloyd, SE, et al.
Publicerad: (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.
av: Nesbit, M, et al.
Publicerad: (2010)