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American Journal of Human Genetics|May 1, 1995
Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 familiesN Doerflinger, C Linder, K Ouahchi, et al.Human Molecular Genetics|September 1, 1993
Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, et al.American Journal of Human Genetics|April 1, 1994
Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markersO Clermont, P Burlet, L Burglen, et al.Neurobiology of Disease|November 1, 1994
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14qG Stevanin, P S Sousa, G Cancel, et al.BMC Systems Biology|October 9, 2008
Iterative reconstruction of a global metabolic model of Acinetobacter baylyi ADP1 using high-throughput growth phenotype and gene essentiality dataMaxime Durot, François Le Fèvre, Véronique de Berardinis, et al.Neurogenetics|November 2, 2004
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3AAnnette Abel, Nuria Fonknechten, Anne Hofer, et al.Nature Genetics|September 1, 1993
A gene for familial hemiplegic migraine maps to chromosome 19A Joutel, M G Bousser, V Biousse, et al.Journal of Immunology (Baltimore, Md. : 1950)|August 18, 2000
Signal transduction of IL-6, leukemia-inhibitory factor, and oncostatin M: structural receptor requirements for signal attenuationD Anhuf, M Weissenbach, J Schmitz, et al.Human Molecular Genetics|January 5, 2002
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1Florence Jobard, Caroline Lefèvre, Aysen Karaduman, et al.Genome Research|May 5, 2001
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8C Charlier, K Segers, D Wagenaar, et al.Pageof 46