Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1)
スポンサーリンク
概要
- 論文の詳細を見る
- 2010-06-01
著者
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Kikuchi Akihiko
Department Of Electrical And Electronics Engineering Sophia University
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Takagi Kimiyo
Department Of Obstetrics And Gynecology Iiyama Red Cross Hospital
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KITA Mariko
Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital
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HARADA Naoki
Kyushu Medical Science
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SHIMOKAWA Osamu
Kyushu Medical Science Nagasaki Laboratory
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Ono Kyoko
Department Of Obstetrics Center For Perinatal Medicine Nagano Children's Hospital
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Horikoshi Tsuguhiro
Department Of Obstetrics Center For Perinatal Medicine Nagano Children's Hospital
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Kawame Hiroshi
Division Of Medical Genetics Center For Perinatal Medicine Nagano Children's Hospital
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Tamaru Shunsuke
Department Of Obstetrics Center For Perinatal Medicine Nagano Children's Hospital
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HORIKOSHI Tsuguhiro
Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital
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MIYASHITA Susumu
Neonatology, Center for Perinatal Medicine, Nagano Children's Hospital
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ONO Kyoko
Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital
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SHIMOKAWA Osamu
Kyushu Medical Science Inc.
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KAWAME Hiroshi
Division of Medical Genetics, Center for Perinatal Medicine, Nagano Children's Hospital
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TAKAGI Kimiyo
Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital
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KITA Mariko
Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital
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HARADA Naoki
Kyushu Medical Science Inc.
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MIYASHITA Susumu
Neonatology, Center for Perinatal Medicine, Nagano Children's Hospital
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Kikuchi Akihiko
Department of Applied Chemistry, Faculty of Engineering, Osaka City University
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