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)

• HORIKOSHI Tsuguhiro

  Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital

• KIKUCHI Akihiko

  Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital

• TAMARU Shunsuke

  Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital

• ONO Kyoko

  Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital

• KITA Mariko

  Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital

• TAKAGI Kimiyo

  Department of Obstetrics, Center for Perinatal Medicine, Nagano Children's Hospital

• MIYASHITA Susumu

  Neonatology, Center for Perinatal Medicine, Nagano Children's Hospital

• KAWAME Hiroshi

  Division of Medical Genetics, Center for Perinatal Medicine, Nagano Children's Hospital

• SHIMOKAWA Osamu

  Kyushu Medical Science Inc.

• HARADA Naoki

  Kyushu Medical Science Inc.

収録刊行物

• The journal of obstetrics and gynaecology research

  The journal of obstetrics and gynaecology research 36 (3), 671-675, 2010-06-01

キーワード

• ARSE
• contiguous gene syndrome
• prenatal diagnosis
• three-dimensional ultrasonography
• X-linked recessive chondrodysplasia punctata

詳細情報

• CRID: 1571980076072515456
• NII論文ID: 10031121675
• NII書誌ID: AA11082002
• ISSN: 13418076
• Web Site: https://search.jamas.or.jp/link/ui/2011079596
• 本文言語コード: en
• データソース種別:
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