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Annals of the Rheumatic Diseases|January 18, 2002
Carriers of the aspartylglucosaminuria genetic mutation and chronic arthritisM Arvio, K Laiho, M Kauppi, et al.Human Genetics|May 1, 1992
Huntington disease in Finland: a molecular and genealogical studyE Ikonen, J Ignatius, R Norio, et al.Archives of Dermatological Research|January 1, 1992
Clinical, light and electron microscopic features of recessive ichthyosis congenita type IIIK M Niemi, L Kanerva, C F Wahlgren, et al.Journal of Medical Genetics|September 1, 1995
Clinical features of nine males with molecularly defined deletions of the Y chromosome long armP Salo, J Ignatius, K O Simola, et al.Pharmacology, Biochemistry, and Behavior|May 1, 1988
Hippocampal rhythmic slow activity in rat lines selected for differences in ethanol-induced motor impairmentP Kaheinen, E R Korpi, I Pyykkö, et al.Journal of Medical Genetics|June 1, 1996
Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3J Ignatius, S Knuutila, S W Scherer, et al.Journal of Medical Genetics|June 17, 2003
A new genetic locus for X linked progressive cone-rod dystrophyR Jalkanen, F Y Demirci, H Tyynismaa, et al.Clinical Dysmorphology|March 15, 2006
Pitt-Hopkins syndrome in two patients and further definition of the phenotypeMaarit M Peippo, Kalle O J Simola, Leena K Valanne, et al.Neuromuscular Disorders : NMD|May 1, 1997
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotypeK Talbot, N R Rodrigues, J Ignatius, et al.Science (New York, N.Y.)|May 22, 1987
Lipoprotein uptake by neuronal growth cones in vitroM J Ignatius, E M Shooter, R E Pitas, et al.Pageof 9