Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13.

Podobne knjige/članki

• LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
  od: Trump, D, et al.
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• Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.
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• 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.
  od: Trump, D, et al.
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• Familial benign hypercalcaemia, Oklahoma variant (FBHok): Localisation to chromosome 19q13.
  od: Lloyd, SE, et al.
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• 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.
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