Variable phenotype and associations in chromosome 22q11.2 microdeletion

Variable phenotype and associations in chromosome 22q11.2 microdeletion

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Veröffentlicht in:American journal of medical genetics. Part A 2006-03, Vol.140A (6), p.659-660
Hauptverfasser: Derbent, Murat, Bikmaz, Yunus Emre, Yilmaz, Zerrin, Tokel, Kursad
Format: Artikel
Sprache:eng
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Chromosome Deletion
Chromosome Disorders - genetics
Chromosomes, Human, Pair 22 - genetics
Down Syndrome - genetics
Heart Defects, Congenital - genetics
Humans
Phenotype
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container_title American journal of medical genetics. Part A
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creator Derbent, Murat
Bikmaz, Yunus Emre
Yilmaz, Zerrin
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doi_str_mv 10.1002/ajmg.a.31120
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source MEDLINE; Wiley Journals
subjects Chromosome Deletion
Chromosome Disorders - genetics
Chromosomes, Human, Pair 22 - genetics
Down Syndrome - genetics
Heart Defects, Congenital - genetics
Humans
Phenotype
title Variable phenotype and associations in chromosome 22q11.2 microdeletion
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