A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies

A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Dobbie, A, Haan, E, Nesbit, M, Bowl, M, Thakker, R
التنسيق:	Journal article
منشور في:	2001

مواد مشابهة

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.
حسب: Nesbit, M, وآخرون
منشور في: (2004)

Molecular diagnosis of hypoparathyroidism: 2 illustrative cases
حسب: Hampson, G, وآخرون
منشور في: (2003)

Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.
حسب: Zahirieh, A, وآخرون
منشور في: (2005)

Clinical case seminar: Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome
حسب: Zahirieh, A, وآخرون
منشور في: (2005)

A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome.
حسب: Gaynor, K, وآخرون
منشور في: (2009)

Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia.
حسب: Bilous, R, وآخرون
منشور في: (1992)

Characteristics of hearing loss in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome.
حسب: Looij, v, وآخرون
منشور في: (2006)

Hypoparathyroidism, sensorineural deafness, and renal dysgenesis syndrome with a mutation
حسب: Yong Suk Shim, وآخرون
منشور في: (2015-03-01)

X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25.
حسب: Bowl, MR, وآخرون
منشور في: (2001)

Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome
حسب: Li Wang, وآخرون
منشور في: (2017-01-01)

Molecular genetics of hypoparathyroidism
حسب: Thakker, R
منشور في: (2003)

Living‐donor kidney transplantation for a patient with hypoparathyroidism, deafness, and renal dysplasia syndrome
حسب: Nobutaka Nishimura, وآخرون
منشور في: (2020-11-01)

A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism.
حسب: Mirczuk, S, وآخرون
منشور في: (2010)

X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.
حسب: Andrew Nesbit, M, وآخرون
منشور في: (2004)

SYNDROME OF HYPOPARATHYROIDISM, DEAFNESS AND RENAL DISEASE (HDR) IN A 7 YEARS OLD BOY AT BAHAWALPUR
حسب: Sumera Akram, وآخرون
منشور في: (2020-10-01)

SYNDROME OF HYPOPARATHYROIDISM, DEAFNESS AND RENAL DISEASE (HDR) IN A 7 YEARS OLD BOY AT BAHAWALPUR
حسب: Sumera Akram, وآخرون
منشور في: (2020-10-01)

Hypoparathyroidism
حسب: Bilezikian, J, وآخرون
منشور في: (1997)

A novel GATA3 frameshift mutation causes hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome
حسب: Bo Huang, وآخرون
منشور في: (2024-03-01)

Genetic developments in hypoparathyroidism.
حسب: Thakker, R
منشور في: (2001)

New candidate genes for X-linked recessive hypoparathyroidism.
حسب: Mumm, S, وآخرون
منشور في: (1999)

A Deaf Child with Hypoparathyroidism: A Case Report
حسب: Fallah R, وآخرون
منشور في: (2010-03-01)

A Deaf Child with Hypoparathyroidism: A Case Report
حسب: R Fallah, وآخرون
منشور في: (2010-04-01)

Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism.
حسب: Bowl, MR, وآخرون
منشور في: (2010)

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.
حسب: Bowl, MR, وآخرون
منشور في: (2005)

Studies of mice deleted for Sox3 and uc482: Relevance to X-linked hypoparathyroidism
حسب: Gaynor, KU, وآخرون
منشور في: (2020)

Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism
حسب: Mannstadt, M, وآخرون
منشور في: (2013)

First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p
حسب: Tumelo M. Satekge, وآخرون
منشور في: (2024-12-01)

Hypoparathyroidism
حسب: Mannstadt, M, وآخرون
منشور في: (2017)

Hypoparathyroidism, sensorineural deafness and renal disease (HDR) syndrome due to a novel GATA3 mutation p.Ala287Asp
حسب: Luke Vroegindewey, وآخرون
منشور في: (2024-12-01)

Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site
حسب: Catarina I. Gonçalves, وآخرون
منشور في: (2023-08-01)

Hypoparathyroidism - A Review of the Molecular Genetic Testing Service in Oxford
حسب: Cranston, T, وآخرون
منشور في: (2008)

Familial hypocalcemia -- not hypoparathyroidism.
حسب: Heath, D
منشور في: (1996)

Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism
حسب: Katherine U Gaynor, وآخرون
منشور في: (2020-02-01)

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.
حسب: Ali, A, وآخرون
منشور في: (2007)

Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3: a case report and review of literature
حسب: Anne D. D. Joseph, وآخرون
منشور في: (2019-10-01)

Spectrum of germline AIRE mutations causing APS-1 and familial hypoparathyroidism
حسب: Cranston, T, وآخرون
منشور في: (2022)

Hypoparathyroidism: genetics and diagnosis
حسب: Mannstadt, M, وآخرون
منشور في: (2022)

Transcription factors in parathyroid development: lessons from hypoparathyroid disorders.
حسب: Grigorieva, I, وآخرون
منشور في: (2011)

Fahr’s Syndrome and Secondary Hypoparathyroidism
حسب: Santos Vitorino Modesto dos, وآخرون
منشور في: (2016-03-01)

Compound heterozygous mutations of the AIRE-1 gene causing autoimmune polyendocrinopathy type 1.
حسب: Bowl, MR, وآخرون
منشور في: (2001)