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Human Genetics|January 1, 1984
Characterization of normal and mutant adenosine deaminase messenger RNAs by translation and hybridization to a cDNA probeG S Adrian, D A Wiginton, J J HuttonHuman Genetics|February 1, 1994
Cystic fibrosis in a low-incidence population: two major mutations in FinlandJ Kere, X Estivill, M Chillón, et al.Human Genetics|March 1, 1994
An additional HpaII polymorphism in exon 2 of the human platelet membrane glycoprotein IIIa geneB Perichon, S Clemenceau, A Romand, et al.Human Genetics|January 1, 1994
Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutationsT Dörk, R Fislage, T Neumann, et al.Human Genetics|January 1, 1994
Detection by the polymerase chain reaction of two polymorphisms in exon 14 of the human inter-alpha-trypsin inhibitor heavy chain H1 geneL Thiberville, J Bourguignon, C Beldjord, et al.Human Genetics|January 1, 1983
Regional localization of the human factor IX gene by molecular hybridizationP F Chance, K A Dyer, K Kurachi, et al.Human Genetics|June 9, 1978
The HLA system and leprosy in ThailandJ Greiner, E Schleiermacher, T Smith, et al.Human Genetics|June 27, 1978
Genetic polymorphism of the second component of human complement (C2): presentation of a modified typing technique and data on C2 phenotype distribution, linkage genetics, and haplotype associations a Norwegian family materialB Olaisen, P Teisberg, T Gedde-Dahl, et al.Human Genetics|June 27, 1978
Patau's syndrome and 13q21q translocationA Pérez-Castillo, J A AbrisquetaPageof 959