KBG SYNDROME DUE TO MUTATIONS IN ANKRD11: COMPLEX CASES OF BLENDED PHENOTYPES, PARENTAL INHERITANCE, AND POTENTIAL PHENOTYPIC EXPANSION TO INCLUDE HEARING LOSS

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• 来源
  《American journal of medical genetics, Part A》 |2018年第6期|共2页
• 作者

  Hurst A. C. E.; Descartes M.; Lose E. J.; Bebin E. M.; Bowling K. M.; Hiatt S. M.; Amaral M. D.; Finnila C. R.; Thompson M. L.; Barsh G. S.; Brothers K. B.; Kelley W. V.; East K. M.; Gray D. E.; Lawlor J. M.; Rich C. A.; Simmons S.; Cannon A.; Skelton T.; Myers R. M.; Korf B. R.; Cooper G. M.;

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• 作者单位

  Univ Alabama Birmingham Birmingham AL USA;

  Univ Alabama Birmingham Birmingham AL USA;

  Univ Alabama Birmingham Birmingham AL USA;

  Univ Alabama Birmingham Birmingham AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  Univ Louisville Louisville KY 40292 USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  Univ Alabama Birmingham Birmingham AL USA;

  Univ Alabama Birmingham Birmingham AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

  Univ Alabama Birmingham Birmingham AL USA;

  HudsonAlpha Inst Biotechnol Huntsville AL USA;

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• 原文格式 PDF
• 正文语种 eng
• 中图分类 医学遗传学;
• 关键词