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Article

De novo deletion of 1q24.3-q31.2 in a patient with severe growth retardation.

American journal of medical genetics. Part A - 1 May 2010

Nishimura Akira, Hiraki Yoko, Shimoda Hiroko, Nishimura Gen, Tadaki Hiromi, Tsurusaki Yoshinori, Miyake Noriko, Saitsu Hirotomo, Matsumoto Naomichi

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Share to Chromosome Banding
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Infant, Newborn

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Identifiers

PMID: 20425845
DOI: 10.1002/ajmg.a.33371

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Related research

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De novo deletion of 1q24.3-q31.2 in a patient with severe growth retardation.PMID 20425845Read ↗

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Nine year old boy with chromosome 1q23.3-q25.1 deletion.Semantic proximity Read ↗

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An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.Semantic proximity Read ↗

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