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Genomics|October 1, 1989
Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophiesH Gilgenkrantz, J Chelly, M Lambert, et al.Journal of Medical Genetics|May 1, 1995
Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomesC Pêcheux, J F Mouret, A Dürr, et al.Human Genetics|October 1, 1986
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophyJ Chelly, F Marlhens, B Le Marec, et al.Archives of Virology|January 1, 1992
Eosinophils as host cells for HIV-1B Conway, P Baskar, L J Bechtel, et al.Annales De Genetique|June 1, 1975
[Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)]M O Rethoré, J C Kaplan, C Junien, et al.Journal of the Neurological Sciences|March 1, 1995
Diagnosis of "sporadic" Huntington's diseaseA Dürr, C Dodé, V Hahn, et al.Annales De Genetique|June 1, 1976
[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12]M O Rethoré, C Junien, G Malpuech, et al.Nature|September 24, 1992
Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.Cancer Genetics and Cytogenetics|August 1, 1982
Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosisC Junien, S Despoisse, C Turleau, et al.Neuromuscular Disorders : NMD|March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.Pageof 19