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Acta Obstetricia Et Gynecologica Scandinavica|April 1, 1995
Prenatal diagnosis of osteogenesis imperfectaL N Berge, V Marton, L Tranebjaerg, et al.European Journal of Human Genetics : EJHG|July 26, 2000
Identification of novel USH2A mutations: implications for the structure of USH2A proteinB Dreyer, L Tranebjaerg, T Rosenberg, et al.Journal of Medical Genetics|October 3, 1999
A new gene (DYX3) for dyslexia is located on chromosome 2T Fagerheim, P Raeymaekers, F E Tønnessen, et al.European Journal of Human Genetics : EJHG|September 26, 2001
Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with AsiaL A Larsen, J Vuust, M Nystad, et al.European Journal of Human Genetics : EJHG|July 6, 2000
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndromeL Tranebjaerg, B C Hamel, F J Gabreels, et al.American Journal of Medical Genetics|July 12, 1996
XLMR genes: update 1996H A Lubs, P Chiurazzi, J F Arena, et al.Annals of Tropical Paediatrics|January 24, 2004
Neonatal morbidity and mortality in a Tanzanian tertiary care referral hospitalC Klingenberg, R Olomi, M Oneko, et al.European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 1, 2014
Colonisation and interaction between S. epidermidis and S. aureus in the nose and throat of healthy adolescentsE G A Fredheim, T Flægstad, F Askarian, et al.Journal of Statistical Physics|November 1, 2021
A Consistent BGK Model with Velocity-Dependent Collision Frequency for Gas MixturesJ Haack, C Hauck, C Klingenberg, et al.The Journal of Biological Chemistry|April 16, 1998
Naturally occurring mutants of human steroid 21-hydroxylase (P450c21) pinpoint residues important for enzyme activity and stabilityA Nikoshkov, S Lajic, A Vlamis-Gardikas, et al.Pageof 11