Document Detail


Partial trisomy 22 resulting from rearrangements between chromosomes 11/22 and 16/22: a report of two cases.
MedLine Citation:
PMID:  12892172     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONCLUSION: Infants with trisomy 22 can present with variable phenotypes. It is important to bear the phenotype of chromosome 22 infants in mind.
Authors:
N Werding; H Holland; D Hueckel; U G Froster; H J Häusler; W Kiess
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Acta paediatrica (Oslo, Norway : 1992)     Volume:  92     ISSN:  0803-5253     ISO Abbreviation:  Acta Paediatr.     Publication Date:  2003 Jul 
Date Detail:
Created Date:  2003-08-01     Completed Date:  2003-12-01     Revised Date:  2013-05-20    
Medline Journal Info:
Nlm Unique ID:  9205968     Medline TA:  Acta Paediatr     Country:  Norway    
Other Details:
Languages:  eng     Pagination:  865-8     Citation Subset:  IM    
Affiliation:
Children's Hospital, University of Leipzig, Leipzig, Germany.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple
Chromosomes, Human, Pair 11 / genetics*
Chromosomes, Human, Pair 16 / genetics*
Chromosomes, Human, Pair 22 / genetics*
DNA Mutational Analysis
Genotype
Humans
Infant, Newborn
Karyotyping
Male
Phenotype
Point Mutation / genetics
Trisomy / genetics*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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