Showing results (1-10 of 207) with videos related to
Sort By:
Pageof 21
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Detection of specific DNA sequences by fluorescence amplification: a color complementation assayF F Chehab, Y W KanLancet (London, England)|January 6, 1990
Detection of sickle cell anaemia mutation by colour DNA amplificationF F Chehab, Y W KanBlood|August 1, 1989
Characterization of a spontaneous mutation in beta-thalassemia associated with advanced paternal ageF F Chehab, K H Winterhalter, Y W KanLancet (London, England)|January 4, 1986
Spontaneous mutation in beta-thalassaemia producing the same nucleotide substitution as that in a common hereditary formF F Chehab, G R Honig, Y W KanModern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 1, 1989
Detection of cytomegalovirus infection in paraffin-embedded tissue specimens with the polymerase chain reactionF F Chehab, X Xiao, Y W Kan, et al.Human Mutation|January 1, 1994
Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacksS P Cai, J Wall, Y W Kan, et al.Blood|January 1, 1993
Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in SicilyA Maggio, A Giambona, S P Cai, et al.Blood|April 1, 1987
The molecular basis of beta-thalassemia in Lebanon: application to prenatal diagnosisF F Chehab, V Der Kaloustian, F P Khouri, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Human placental Na+,K+-ATPase alpha subunit: cDNA cloning, tissue expression, DNA polymorphism, and chromosomal localizationF F Chehab, Y W Kan, M L Law, et al.Pageof 21