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Clinical Chemistry|September 1, 1989
Use of polymerase chain reaction for diagnosis of inherited disordersC D BoehmBlood|October 1, 1988
Molecular basis and prenatal diagnosis of beta-thalassemiaH H Kazazian, C D BoehmThe Journal of Pediatrics|March 1, 1992
Familial neurofibromatosis type 1: clinical experience with DNA testingK J Hofman, C D BoehmCurrent Opinion in Biotechnology|December 11, 1990
The molecular basis of genetic diseaseC D Boehm, H H KazazianHuman Genetics|January 1, 1984
Prenatal detection of an unstable ring 21 chromosomeG Stetten, B Sroka, V L Corson, et al.Blood|August 1, 1988
Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletionR Anand, C D Boehm, H H Kazazian, et al.Blood|December 23, 1999
Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemiaS S Chong, C D Boehm, D R Higgs, et al.Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|August 1, 1993
Increased echogenicity in the fetal abdomen: use of DNA analysis to establish a diagnosis of cystic fibrosisW A Hogge, J S Hogge, C D Boehm, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1982
Nonrandom association of polymorphic restriction sites in the beta-globin gene clusterS E Antonarakis, C D Boehm, P J Giardina, et al.American Journal of Physical Anthropology|January 1, 1990
Phylogeny of human beta-globin haplotypes and its implications for recent human evolutionJ C Long, A Chakravarti, C D Boehm, et al.Pageof 4