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Shinji Kondoh

Nagasaki University

3

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Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family

2008 Journal of Human Genetics
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Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia

2005 American Journal of Medical Genetics Part A
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A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet

2002 Journal of Human Genetics
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