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Annals of Medicine|February 1, 1993
Human gene mutations affecting RNA processing and translationD N CooperHuman Genetics|July 8, 1998
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delayM Upadhyaya, M Ruggieri, J Maynard, et al.Forensic Science International|April 20, 2001
Population genetics of Y-chromosomal microsatellites in Baltic malesR Lessig, J Edelmann, M KrawczakAmerican Journal of Human Genetics|September 1, 1992
Likelihoods of multilocus DNA fingerprints in extended familiesB Bockel, P Nürnberg, M KrawczakHuman Genetics|May 1, 1997
Characterization and significance of nine novel mutations in exon 16 of the neurofibromatosis type 1 (NF1) geneJ Maynard, M Krawczak, M UpadhyayaHuman Genetics|February 1, 1988
Linkage of the DNA-segment D7S13 (pB79a) with the cystic fibrosis locusD Böhm, M Krawczak, J SchmidtkeTechniques in Coloproctology|March 9, 2017
Five years of experience with the FiLaC™ laser for fistula-in-ano management: long-term follow-up from a single institutionA Wilhelm, A Fiebig, M KrawczakNucleic Acids Research|April 25, 1991
A comprehensive list of cloned human DNA sequences--1990 updateJ Schmidtke, D N CooperHuman Genetics|February 1, 1988
The CpG dinucleotide and human genetic diseaseD N Cooper, H YoussoufianNucleic Acids Research|April 25, 1990
A comprehensive list of cloned human DNA sequencesJ Schmidtke, D N CooperPageof 26