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Fungal Genetics and Biology : FG & B|August 2, 2003
Characterization of the genomic organization of the region bordering the centromere of chromosome V of Podospora anserina by direct sequencingPhilippe Silar, Christian Barreau, Robert Debuchy, et al.Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.American Journal of Human Genetics|September 1, 1996
Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French CanadiansM Labuda, D Labuda, M Korab-Laskowska, et al.BMC Genomics|May 18, 2007
Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysisAna C Fierro, Raphaël Thuret, Laurent Coen, et al.American Journal of Human Genetics|April 1, 1996
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3pJ A Kaukonen, P Amati, A Suomalainen, et al.Environmental Microbiology|May 8, 2008
Discovery and characterization of a new bacterial candidate division by an anaerobic sludge digester metagenomic approachSonda Guermazi, Patrick Daegelen, Catherine Dauga, et al.American Journal of Human Genetics|December 1, 1994
Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patientA F Lewanda, E D Green, J Weissenbach, et al.Nature Genetics|March 1, 1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12E Tournier-Lasserve, A Joutel, J Melki, et al.Proceedings of the National Academy of Sciences of the United States of America|June 15, 2022
Denitrification in foraminifera has an ancient origin and is complemented by associated bacteriaChristian Woehle, Alexandra-Sophie Roy, Nicolaas Glock, et al.American Journal of Human Genetics|March 11, 2000
Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneityJ Fischer, A Faure, B Bouadjar, et al.Pageof 46