检索结果 - AF Markham
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Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss 由 DA Scott, ML Kraft, Rivka Carmi, A. Ramesh, Khalil Elbedour, Yael Yairi, C. R. Srikumari Srisailapathy, S. Rosengren, AF Markham, Mueller Rf, Nicholas Lench, Guy Van Camp, Richard J. Smith, Val C. Sheffield
出版 1998Artigo
相关主题
Biology
Gene
Genetics
Allele
Antigen
Audiology
Cancer
Cancer research
Carcinoma
Chromoplexy
Coding region
Epitope
Frameshift mutation
Hearing loss
Immunology
LNCaP
Locus (genetics)
Malignancy
Medicine
Mutation
PCA3
Phenotype
Prostate
Prostate cancer
Prostate-specific antigen
Single-strand conformation polymorphism
Stop codon