Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 140A; no. 4; pp. 388 - 391
Main Authors Shrimpton, Antony E., Jensen, Kimberly A., Hoo, Joe J.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.02.2006
Wiley-Liss
Subjects
Biological and medical sciences
Child, Preschool
Chromosome Banding
Chromosome Deletion
Chromosomes, Human, Pair 3 - genetics
Chromosomes, Human, Pair 8 - genetics
Classical genetics, quantitative genetics, hybrids
Cognition Disorders - diagnosis
Cognition Disorders - genetics
Fundamental and applied biological sciences. Psychology
Gene Duplication
Genetics of eukaryotes. Biological and molecular evolution
Human
Humans
In Situ Hybridization, Fluorescence
Karyotyping
Male
Phenotype
Chromosomal aberration
Genetic mapping
Case study
Phenotype
Cognitive disorder
Cytogenetics
Deletion
Abnormal chromosome
Molecular biology
Chromosome duplication
Normal
Karyotype
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Bibliography:istex:9B805571E0BD7EE679E6D9083B6CD75B3C68A85C
ArticleID:AJMG31066
ark:/67375/WNG-WW8MGX35-G
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.31066