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American Journal of Human Genetics|March 1, 1986
Regional mapping of six cloned DNA sequences on human chromosome 7I Bartels, K H Grzeschik, D N Cooper, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|November 1, 1985
[Familial, structural aberration of the Y chromosome with fertility disorders]H Gall, M Schmid, J Schmidtke, et al.Artificial Organs|November 1, 1982
Advantages of bicarbonate hemodialysisH Hampl, H Klopp, M Wolfgruber, et al.Brain & Development|November 1, 1991
Multiple sclerosis in childhood: report of 15 casesF Hanefeld, H J Bauer, H J Christen, et al.Pediatric Neurology|August 30, 2000
Quantitative proton magnetic resonance spectroscopy of focal brain lesionsB Wilken, P Dechent, J Herms, et al.Journal of Medical Genetics|December 24, 1998
Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28T Webb, A Clarke, F Hanefeld, et al.European Journal of Endocrinology|July 1, 1997
Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findingsG C Korenke, C Roth, E Krasemann, et al.Neuropediatrics|October 9, 2002
Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patientsM Meins, K Brockmann, S Yadav, et al.Developmental Medicine and Child Neurology|March 4, 2000
Foix-Chavany-Marie (anterior operculum) syndrome in childhood: a reappraisal of Worster-Drought syndromeH J Christen, F Hanefeld, E Kruse, et al.American Journal of Human Genetics|April 20, 2001
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal originR Trappe, F Laccone, J Cobilanschi, et al.Pageof 33