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European Journal of Human Genetics : EJHG|February 15, 2001
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in ScandinaviaJ Jonasson, V Juvonen, P Sistonen, et al.Genomics|February 1, 1992
Linkage analysis of spinal muscular atrophyR J Daniels, N H Thomas, R N MacKinnon, et al.Journal of Medical Genetics|February 1, 1995
Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null alleleR J Daniels, L Campbell, N R Rodrigues, et al.Human Genetics|September 1, 1993
Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA)K E Morrison, R J Daniels, G K Suthers, et al.Journal of Medical Genetics|July 3, 2007
Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arraysJuliane Hoyer, Alexander Dreweke, Christian Becker, et al.Genetic Epidemiology|February 17, 2001
Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-populationK Pääkkönen, S Sauramo, L Sarantaus, et al.Human Molecular Genetics|November 5, 1997
Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated populationT Laitinen, P Kauppi, J Ignatius, et al.Clinical Genetics|August 8, 2009
Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutationsM Encarnação, L Lacerda, R Costa, et al.The Journal of Clinical Investigation|March 1, 1989
A role for apolipoprotein E, apolipoprotein A-I, and low density lipoprotein receptors in cholesterol transport during regeneration and remyelination of the rat sciatic nerveJ K Boyles, C D Zoellner, L J Anderson, et al.American Journal of Human Genetics|April 17, 2007
Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome)Christiane Zweier, Maarit M Peippo, Juliane Hoyer, et al.Pageof 9