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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.Human Mutation|March 10, 2001
Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regionsF Laccone, P Huppke, F Hanefeld, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Fetal alcohol syndrome in association with Rett syndromeB Zoll, P Huppke, A Wessel, et al.Neuropediatrics|June 21, 2002
Altered methylation pattern of the G6 PD promoter in Rett syndromeP Huppke, S Bohlander, N Krämer, et al.Human Molecular Genetics|May 18, 2000
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patientsP Huppke, F Laccone, N Krämer, et al.Neuropediatrics|June 21, 2002
Influence of mutation type and location on phenotype in 123 patients with Rett syndromeP Huppke, M Held, F Hanefeld, et al.Clinical Dysmorphology|January 29, 2000
Two brothers with Hennekam syndrome and cerebral abnormalitiesP Huppke, H J Christen, B Sattler, et al.The British Journal of Dermatology|June 10, 2000
Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?S Schauder, F Hanefeld, U M Noske, et al.Acta Paediatrica (Oslo, Norway : 1992)|January 26, 2002
Endocrinological study on growth retardation in Rett syndromeP Huppke, C Roth, H J Christen, et al.Journal of Medical Genetics|May 13, 2006
Very mild cases of Rett syndrome with skewed X inactivationP Huppke, E M Maier, A Warnke, et al.Pageof 26