Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 152A; no. 12; pp. 3185 - 3188
Main Authors Shanske, A.L., Leonard, J., Nahum, O., Coppock, D.L., Levy, B.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.12.2010
Wiley-Liss
Subjects
Biological and medical sciences
Child, Preschool
Chromosome aberrations
Chromosome Breakage
Chromosome Duplication
Chromosomes, Human, Pair 3
Classical genetics, quantitative genetics, hybrids
Cytogenetic Analysis
DNA Copy Number Variations
Fundamental and applied biological sciences. Psychology
Gene Dosage
Genetics of eukaryotes. Biological and molecular evolution
Human
Humans
Male
Medical genetics
Medical sciences
Oligonucleotide Array Sequence Analysis - methods
Phenotype
Polymorphism, Single Nucleotide
Chromosomal aberration
Genetic mapping
Breakpoint
Chromosome break
Abnormal chromosome
Boundary value
Chromosome duplication
De novo
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Bibliography:istex:9D8B817FD8674E187C3EF60A917CB97B100B0DAD
How to Cite this Article: Shanske AL, Leonard J, Nahum O, Coppock DL, Levy B. 2010. Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA. Am J Med Genet Part A 152A:3185-3188.
ark:/67375/WNG-2FS1Z4DF-1
ArticleID:AJMG33431
How to Cite this Article: Shanske AL, Leonard J, Nahum O, Coppock DL, Levy B. 2010. Delineation of the breakpoints of pure duplication 3q due to a de novo duplication event using SOMA. Am J Med Genet Part A 152A:3185–3188.
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ISSN:1552-4825
1552-4833
1552-4833
DOI:10.1002/ajmg.a.33431