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Human Molecular Genetics|August 25, 2000
Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesisA Kerjean, J M Dupont, C Vasseur, et al.Annales De Genetique|January 1, 1988
Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndromeI Henry, M Jeanpierre, F Barichard, et al.Neuromuscular Disorders : NMD|March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.Human Molecular Genetics|December 1, 1994
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patientsP Miniou, M Jeanpierre, V Blanquet, et al.Annales De Genetique|January 1, 1997
PEG1 expression in maternal uniparental disomy 7L Cuisset, C Le Stunff, J M Dupont, et al.Nature Genetics|June 1, 1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severityF Piccolo, S L Roberds, M Jeanpierre, et al.Cytogenetics and Cell Genetics|July 7, 1999
Abnormal methylation does not prevent X inactivation in ICF patientsD Bourc'his, P Miniou, M Jeanpierre, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan geneA Lasa, F Piccolo, C de Diego, et al.The Journal of Clinical Investigation|January 1, 1994
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophinK Matsumura, A H Burghes, M Mora, et al.Human Genetics|May 1, 1992
Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD)B Müller, C Dechant, G Meng, et al.Pageof 6