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
Molecular diagnosis of hypopar...
Cite this
Text this
Email this
Print
Export Record
Export to RefWorks
Export to EndNoteWeb
Export to EndNote
Permanent link
Molecular diagnosis of hypoparathyroidism: 2 illustrative cases
Bibliographic Details
Main Authors:
Hampson, G
,
Bowl, MR
,
Nesbit, M
,
Giannoulis, M
,
Jones, R
,
Thakker, R
Format:
Conference item
Published:
2003
Holdings
Description
Similar Items
Staff View
Similar Items
A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
by: Dobbie, A, et al.
Published: (2001)
X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25.
by: Bowl, MR, et al.
Published: (2001)
A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism.
by: Mirczuk, S, et al.
Published: (2010)
Molecular genetics of hypoparathyroidism
by: Thakker, R
Published: (2003)
X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.
by: Andrew Nesbit, M, et al.
Published: (2004)