机译:APCDD1是一种新型Wnt抑制剂,在遗传性单纯性遗传不足中发生了突变
Department of Dermatology,Columbia University, College of Physicians and Surgeons, 630 West 168th Street, VC15 204A, New York,New York 10032, USA;
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
The Laboratory of Vertebrate Embryology, The Rockefeller University,New York, New York 10065, USA;
Department of Dermatology,Columbia University, College of Physicians and Surgeons, 630 West 168th Street, VC15 204A, New York,New York 10032, USA Department of Genetics and Development, Columbia University, College of Physicians and Surgeons, 630 West 168th Street, VC15 204A, New York,New York 10032, USA;
Department of Dermatology,Columbia University, College of Physicians and Surgeons, 630 West 168th Street, VC15 204A, New York,New York 10032, USA;
Institute of Medical Genetics, University of Zurich, Schwerzenbach CH-8603, Switzerland;
Struttura Semplice Genetica Medica APSS, Trento 138100, Italy;
Department of Dermatology,Columbia University, College of Physicians and Surgeons, 630 West 168th Street, VC15 204A, New York,New York 10032, USA;
Institute of Medical Genetics, University of Zurich, Schwerzenbach CH-8603, Switzerland;
The Laboratory of Vertebrate Embryology, The Rockefeller University,New York, New York 10065, USA;
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
Department of Dermatology,Columbia University, College of Physicians and Surgeons, 630 West 168th Street, VC15 204A, New York,New York 10032, USA Department of Genetics and Development, Columbia University, College of Physicians and Surgeons, 630 West 168th Street, VC15 204A, New York,New York 10032, USA;
机译:APCDD1基因的反复突变导致一个中国大家庭的遗传性单纯性遗传不足
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机译:APCDD1是一种新型WNT抑制剂在遗传性腹下椎间盘病变外
机译:APCDD1是一种新型Wnt抑制剂,在遗传性单纯性遗传不足中发生了突变