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Molecular and Cellular Probes|October 21, 1998
Molecular analysis reveals a high mutation frequency in the first untranslated exon of the PPOX gene and largely excludes variegate porphyria in a subset of clinically affected Afrikaner familiesM J Kotze, J N De Villiers, J Z Groenewald, et al.Nature Genetics|July 1, 1996
Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancersS Thiagalingam, C Lengauer, F S Leach, et al.Human Molecular Genetics|July 1, 1996
Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyriaL Warnich, M J Kotze, I M Groenewald, et al.American Journal of Medical Genetics|April 9, 1996
Neuropsychiatry of 18q- syndromeR N Mahr, P J Moberg, J Overhauser, et al.Genomics|December 28, 1999
Physical map and characterization of transcripts in the candidate interval for familial chondrocalcinosis at chromosome 5p15.1K Rojas, L Serrano de la Peña, T Gallardo, et al.Pageof 13