| Pseudohypoparathyroidism associated with cri du chat syndrome. | |
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MedLine Citation:
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PMID: 995018 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A case is reported in which features of pseudohypoparathyroidism were found in association with the cri du chat syndrome. This association may throw some light on the localization of the chromosomal abberration which underlies pseudohypoparathyroidism, since deletion of the short arm of chromosome 5 has been clearly established in the cri du chat syndrome. |
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Authors:
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C W Kee; P Lim; I K Tan |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: The Medical journal of Australia Volume: 2 ISSN: 0025-729X ISO Abbreviation: Med. J. Aust. Publication Date: 1976 Aug |
Date Detail:
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Created Date: 1977-01-25 Completed Date: 1977-01-25 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 0400714 Medline TA: Med J Aust Country: AUSTRALIA |
Other Details:
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Languages: eng Pagination: 344-5 Citation Subset: IM |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Adolescent Child Chromosome Deletion Chromosomes, Human, 4-5 Cri-du-Chat Syndrome / complications*, genetics Female Humans Male Pseudohypoparathyroidism / complications*, genetics |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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