Pendred's syndrome: identification of the genetic defect a century after its recognition.
about
Pendrin: an apical Cl-/OH-/HCO3- exchanger in the kidney cortexThe spectrum of thyroid diseases in childhood and its evolution during transition to adulthood: natural history, diagnosis, differential diagnosis and management.The sodium iodide symporter: its pathophysiological and therapeutic implications.Detection of mutations in genes associated with hearing loss using a microarray-based approach.SLC26A4 gene copy number variations in Chinese patients with non-syndromic enlarged vestibular aqueduct.Comparison of MRI findings with traditional criteria in diagnosis of Pendred syndrome.[Enzymes involved in thyroid iodide organification].Syndromic Hearing Loss: A Brief Review of Common Presentations and Genetics.Expression of human pendrin in diseased thyroids.
P2860
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P2860
Pendred's syndrome: identification of the genetic defect a century after its recognition.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@ast
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@en
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@nl
type
label
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@ast
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@en
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@nl
prefLabel
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@ast
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@en
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@nl
P356
P1433
P1476
Pendred's syndrome: identification of the genetic defect a century after its recognition.
@en
P2093
P356
10.1089/THY.1999.9.65
P577
1999-01-01T00:00:00Z