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American Journal of Human Genetics|March 11, 2000
A recurrent expansion of a maternal allele with 36 CAG repeats causes Huntington disease in two sistersF Laccone, W ChristianHuman Mutation|July 17, 1999
A fast polymerase chain reaction-mediated strategy for introducing repeat expansions into CAG-repeat containing genesF Laccone, R Maiwald, S BingemannHuman 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.Der Urologe. Ausg. A|July 1, 1995
[Congenital agenesis of the vas deferens and cystic fibrosis]A Kugler, F Laccone, W Weidner, et al.Clinical Genetics|November 9, 2013
Detection of 15 novel mutations in 52 children from 40 families with the Marfan or Loeys-Dietz syndrome and phenotype-genotype correlationsC Pees, I Michel-Behnke, M Hagl, et al.Neuropediatrics|June 21, 2002
Altered methylation pattern of the G6 PD promoter in Rett syndromeP Huppke, S Bohlander, N Krämer, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Fetal alcohol syndrome in association with Rett syndromeB Zoll, P Huppke, A Wessel, 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.European Journal of Human Genetics : EJHG|April 10, 1999
A European pilot quality assessment scheme for molecular diagnosis of Huntington's diseaseM Losekoot, B Bakker, F Laccone, 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.Pageof 4