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

Detalhes bibliográficos
Main Authors: Dobbie, A, Haan, E, Nesbit, M, Bowl, M, Thakker, R
Formato: Journal article
Publicado em: 2001
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author Dobbie, A
Haan, E
Nesbit, M
Bowl, M
Thakker, R
author_facet Dobbie, A
Haan, E
Nesbit, M
Bowl, M
Thakker, R
author_sort Dobbie, A
collection OXFORD
description
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format Journal article
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institution University of Oxford
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publishDate 2001
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spelling oxford-uuid:91db4a4d-c9ba-4d38-a915-afeee738b09b2022-03-26T23:21:28ZA family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studiesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:91db4a4d-c9ba-4d38-a915-afeee738b09bSymplectic Elements at Oxford2001Dobbie, AHaan, ENesbit, MBowl, MThakker, R
spellingShingle Dobbie, A
Haan, E
Nesbit, M
Bowl, M
Thakker, R
A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
title A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
title_full A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
title_fullStr A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
title_full_unstemmed A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
title_short A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
title_sort family with hypoparathyroidism deafness and renal anomaly syndrome clinical and molecular studies
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