The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene
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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2004-06-01
著者
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Mulley John
Department Of Genetic Medicine Women's And Children's Hospital And Department Of Molecular
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Mulley John
Department Of Genetic Medicine Women's And Children's Hospital
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Mulley John
Department Of Cytogenetics And Molecular Genetics Centre For Medical Genetics Women's And Child
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Mckenzie Olivia
Department Of Genetic Medicine Women's And Children's Hospital
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Eyre Helen
Department Of Genetic Medicine Women's And Children's Hospital
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BHALLA Kavita
Department of Genetic Medicine, Women's and Children's Hospital
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PHILLIPS Hilary
Department of Genetic Medicine, Women's and Children's Hospital
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CRAWFORD Joanna
Department of Genetic Medicine, Women's and Children's Hospital
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GARDNER Alison
Department of Genetic Medicine, Women's and Children's Hospital
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KREMMIDIOTIS Gabriel
Department of Genetic Medicine, Women's and Children's Hospital
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CALLEN David
Department of Medicine, Breast Cancer Genetics Group, Hanson Institute (North Building), Institute o
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Callen David
Department Of Medicine Breast Cancer Genetics Group Hanson Institute (north Building) Institute Of M
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Bhalla Kavita
Department Of Genetic Medicine Women's And Children's Hospital
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Gardner Alison
Department Of Genetic Medicine Women's And Children's Hospital
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Crawford Joanna
Department Of Genetic Medicine Women's And Children's Hospital
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Phillips Hilary
Department Of Genetic Medicine Women's And Children's Hospital
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Kremmidiotis Gabriel
Department Of Genetic Medicine Women's And Children's Hospital
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- The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene
- Genetic Association Studies in Epilepsy : "The Truth Is Out There"
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