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Nucleic Acids Research|August 1, 1998
Two color hybridization analysis using high density oligonucleotide arrays and energy transfer dyesJ G Hacia, K Edgemon, B Sun, et al.American Journal of Medical Genetics|May 1, 1986
Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapyG N Wilson, R G Holmes, J Custer, et al.American Journal of Medical Genetics|August 14, 1995
17q inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type oneA Asamoah, K North, S Doran, et al.Genomics|March 1, 1990
Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12T A Donlon, A M Krensky, M R Wallace, et al.Nature|January 24, 1985
A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobinF S Collins, J E Metherall, M Yamakawa, et al.Genomics|April 10, 1995
Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pterC Wijmenga, N A Speck, N C Dracopoli, et al.Proceedings of the National Academy of Sciences of the United States of America|May 27, 1997
Human BRCA1 inhibits growth in yeast: potential use in diagnostic testingJ S Humphrey, A Salim, M R Erdos, et al.Genomics|May 1, 1988
Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresisM L Drumm, C L Smith, M Dean, et al.Annals of Internal Medicine|September 12, 1998
Multiple endocrine neoplasia type 1: clinical and genetic topicsS Marx, A M Spiegel, M C Skarulis, et al.Nature|April 23, 1992
Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patientsT N Basu, D H Gutmann, J A Fletcher, et al.Pageof 24