Hypothyroidism and Chromosome 21 Deletion

A 12-year-old mentally retarded girl with a large deletion of the long arm of chromosome 21 and congenital hypothyroidism is reported from the Department of Clinical Genetics and Pediatrics, University Hospital, Uppsala, Sweden.

Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 1996-09-01
Series:Pediatric Neurology Briefs
Subjects:
Online Access:https://www.pediatricneurologybriefs.com/articles/3722
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spelling doaj-e56231550c40457bac1aab88253eefe62020-11-25T02:04:16ZengPediatric Neurology Briefs PublishersPediatric Neurology Briefs1043-31552166-64821996-09-01109707110.15844/pedneurbriefs-10-9-103708Hypothyroidism and Chromosome 21 DeletionJ Gordon Millichap0Northwestern University Feinberg School of MedicineA 12-year-old mentally retarded girl with a large deletion of the long arm of chromosome 21 and congenital hypothyroidism is reported from the Department of Clinical Genetics and Pediatrics, University Hospital, Uppsala, Sweden.https://www.pediatricneurologybriefs.com/articles/3722congenital hypothyroidismdown syndromechromosome 21
collection DOAJ
language English
format Article
sources DOAJ
author J Gordon Millichap
spellingShingle J Gordon Millichap
Hypothyroidism and Chromosome 21 Deletion
Pediatric Neurology Briefs
congenital hypothyroidism
down syndrome
chromosome 21
author_facet J Gordon Millichap
author_sort J Gordon Millichap
title Hypothyroidism and Chromosome 21 Deletion
title_short Hypothyroidism and Chromosome 21 Deletion
title_full Hypothyroidism and Chromosome 21 Deletion
title_fullStr Hypothyroidism and Chromosome 21 Deletion
title_full_unstemmed Hypothyroidism and Chromosome 21 Deletion
title_sort hypothyroidism and chromosome 21 deletion
publisher Pediatric Neurology Briefs Publishers
series Pediatric Neurology Briefs
issn 1043-3155
2166-6482
publishDate 1996-09-01
description A 12-year-old mentally retarded girl with a large deletion of the long arm of chromosome 21 and congenital hypothyroidism is reported from the Department of Clinical Genetics and Pediatrics, University Hospital, Uppsala, Sweden.
topic congenital hypothyroidism
down syndrome
chromosome 21
url https://www.pediatricneurologybriefs.com/articles/3722
work_keys_str_mv AT jgordonmillichap hypothyroidismandchromosome21deletion
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