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Human Genetics|September 12, 2000
An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del(15)(q11q13) in a Finnish familyH Kokkonen, J LeistiHuman Genetics|May 1, 1995
A molecular and cytogenetic study in Finnish Prader-Willi patientsH Kokkonen, M Kähkönen, J LeistiScandinavian Journal of Rheumatology|June 22, 2010
Influence of female hormonal factors, in relation to autoantibodies and genetic markers, on the development of rheumatoid arthritis in northern Sweden: a case-control studyE Berglin, H Kokkonen, E Einarsdottir, et al.Biomacromolecules|August 6, 2008
Differentiation of osteoblasts on pectin-coated titaniumH Kokkonen, C Cassinelli, R Verhoef, et al.Annals of Neurology|February 24, 2001
Decreased binding of [11C]flumazenil in Angelman syndrome patients with GABA(A) receptor beta3 subunit deletionsI E Holopainen, E L Metsähonkala, H Kokkonen, et al.Clinical Genetics|June 29, 2017
A homozygous I684T in GLE1 as a novel cause of arthrogryposis and motor neuron lossT Paakkola, K Vuopala, H Kokkonen, et al.American Journal of Human Genetics|February 11, 1999
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutationT Ohta, K Buiting, H Kokkonen, et al.American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.Pageof 1