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Cytogenetics and Cell Genetics|January 1, 1993
An irradiation-reduced hybrid panel for fine-structure mapping of the Xq28 region in the human genomeB Peterlin, A Smahi, L Holvoet-Vermaut, et al.Genomics|November 1, 1989
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locusA Vincent, N Dahl, I Oberlé, et al.Neuromuscular Disorders : NMD|August 1, 1996
X-linked myotubular myopathy: refinement of the critical gene regionZ Smolenicka, J Laporte, L Hu, et al.American Journal of Medical Genetics|September 1, 1992
Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type IIM Beck, C Steglich, B Zabel, et al.Acta Neurologica Scandinavica|March 5, 2010
Re-evaluation of the dysequilibrium syndromeA Melberg, H Orlén, R Raininko, et al.American Journal of Medical Genetics|December 1, 1992
Infantile autism--fragile X: molecular findings support genetic heterogeneityH Malmgren, K H Gustavson, J Wahlström, et al.Neuropsychobiology|October 10, 2006
Constitutional downregulation of SEMA5A expression in autismM Melin, B Carlsson, H Anckarsater, et al.European Journal of Cancer (Oxford, England : 1990)|July 19, 2000
Prognosis and clinical presentation of BRCA2-associated breast cancerN Loman, O Johannsson, P Bendahl, et al.Human Molecular Genetics|July 1, 1997
Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunctionN Dahl, M Pigg, E Ristoff, et al.American Journal of Human Genetics|August 27, 1998
Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish familyJ Balciuniene, N Dahl, E Borg, et al.Pageof 14