エナメル質欠損症における遺伝子解析
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Bibliographic Information
エナメル質欠損症における遺伝子解析
中込弥男, 1994
- Title Transcription
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エナメルシツ ケッソンショウ ニ オケル イデンシ カイセキ
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Note
平成5年度科学研究費補助金(一般研究B)研究成果報告書
研究課題番号: 03454501
研究分担者: 中堀豊
Contents of Works
- A human X-Y homologous region encodes "Amelogenin" / Yutaka Nakahori[ほか]
- A deletion in the Amelogenin gene (AMG) causes X-linked Amelogenesis imperfecta (AIH1) / Maria Lagerstoem[ほか]
- Short communication : molecular cloning and mapping of 10 new probes on the human Y chromosome / Y. Nakahori[ほか]
- Sex identification by polymerase chain reaction using X-Y homologous primer / Yutaka Nakahori[ほか]
- PCR detection of structurally abnormaly chromosomes / Shigeo Nagafuchi[ほか]
- PCR detection of distal Yp sequences in an XX true hermaphrodite / Yasuo Nakagome[ほか]
- Absence of fetal cells maternal circulation at a level of 1 in 25,000 / Yasuo Nakagome[ほか]
- Sex determination of forensic samples by dual PCR amplification of an X-Y homologous gene / Atsushi Akane[ほか]
- The majority of the marker chromosomes in Japanese patients with stigmata of Turner syndrome are derived from Y chromosomes / Shigeo Nagafuchi[ほか]
