MCDONALD Merry-Lynn | Department of Molecular and Human Genetics, Baylor College of Medicine

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概要

• MCDONALD Merry-Lynnの詳細を見る
• 同名の論文著者
• Department of Molecular and Human Genetics, Baylor College of Medicineの論文著者

関連著者

• AHMAD Wasim

  Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University

• Chishti Muhammad

  Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University

• Ahmad Wasim

  Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University

• MCDONALD Merry-Lynn

  Department of Molecular and Human Genetics, Baylor College of Medicine

• LEAL Suzanne

  Department of Molecular and Human Genetics, Baylor College of Medicine

• Leal Suzanne

  Department Of Molecular And Human Genetics Baylor College Of Medicine

• Lee Kwanghyuk

  Department Of Molecular And Human Genetics Baylor College Of Medicine

• Mcdonald Merry-lynn

  Department Of Molecular And Human Genetics Baylor College Of Medicine

• Chishti Muhammad

  Department Of Biochemistry Quaid-i-azam University

• Chishti Muhammad

  パキスタン

• ANSAR Muhammad

  Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University

• BHATTI Attya

  Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University

• TAMIM Sana

  Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University

• LEE Kwanghyuk

  Department of Molecular and Human Genetics, Baylor College of Medicine

• Tamim Sana

  Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University

• Bhatti Attya

  Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University

• Hassan Muhammad

  Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University

• Ansar Muhammad

  Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University

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著作論文

• Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families
• Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3

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