Skip to content
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文（繁體）
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Language
All Fields
Title
Author
Subject
Call Number
ISBN/ISSN
Tag
Find
Advanced
Genetic mapping studies of fam...
Cite this
Text this
Email this
Print
Export Record
Export to RefWorks
Export to EndNoteWeb
Export to EndNote
Permanent link
Genetic mapping studies of familial benign hypercalcemia type 3 (FBH3) on chromosome 19q13.
Bibliographic Details
Main Authors:
Cianferotti, L
,
Pannett, A
,
Whyte, M
,
Thakker, R
Format:
Journal article
Published:
1999
Holdings
Description
Similar Items
Staff View
Similar Items
LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
by: Trump, D, et al.
Published: (1995)
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.
by: Lloyd, SE, et al.
Published: (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.
by: Trump, D, et al.
Published: (1995)
Familial benign hypercalcaemia, Oklahoma variant (FBHok): Localisation to chromosome 19q13.
by: Lloyd, SE, et al.
Published: (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.
by: Nesbit, M, et al.
Published: (2010)