A simple method for calculating risks before DNA analysisJEANPIERRE, M.Journal of medical genetics. 1988, Vol 25, Num 10, pp 663-668, issn 0022-2593Article

Germinal mosaicism and risk calculation in X-linked diseasesJEANPIERRE, M.American journal of human genetics. 1992, Vol 50, Num 5, pp 960-967, issn 0002-9297Article

Mutation causale ou polymorphisme rare ? La fréquence d'une mutation non retrouvée sur n chromosomes est inférieure à 3/n = Pathologenic mutation or low-frequency polmymorphism ? Frequency of a DNA variant not found in n chromosomes is less than 3/nJEANPIERRE, M.Annales de génétique (Paris). 1996, Vol 39, Num 3, pp 133-138, issn 0003-3995Article

Human satellites 2 and 3JEANPIERRE, M.Annales de génétique (Paris). 1994, Vol 37, Num 4, pp 163-171, issn 0003-3995Article

A rapid method for the purification of DNA from bloodJEANPIERRE, M.Nucleic acids research. 1987, Vol 15, Num 22, issn 0305-1048, 9611Article

CONSTRUCTION AND CHARACTERIZATION OF GENOMIC LIBRARIES FROM SPECIFIC HUMAN CHROMOSOMES = CONSTRUCTION ET CARACTERISATION DE BANQUES DE GENOMES A PARTIR DE CHROMOSOMES HUMAINS SPECIFIQUESKRUMLAUF R; JEANPIERRE M; YOUNG BD et al.1982; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1982; VOL. 79; NO 9; PP. 2971-2975; BIBL. 31 REF.Article

Etablissement de l'empreinte parentale dans la lignée germinale. Conséquences pour la prise en charge en AMP = Imprinting in the germ line. Consequences for assisted reproductionKERJEAN, A; JEANPIERRE, M; JOUANNET, P et al.Andrologie (Lille). 2001, Vol 11, Num 4, pp 209-220, issn 1166-2654Conference Paper

Le conseil génétique et le diagnostic prénatal dans la myopathie de Duchenne: hier, aujourd'hui et demain = Genetic counselling and prenatal diagnosis in Duchenne muscular distrophy: yesterday, today and tomorrowKAPLAN, J; BRIARD, M. L; JEANPIERRE, M et al.Journal de génétique humaine. 1987, Vol 35, Num 1, pp 3-18, issn 0021-7743Article

The organization of two related subfamilies of a human tandemly repeated DNA is chromosome specificJEANPIERRE, M; WEIL, D; GALLANO, P et al.Human genetics. 1985, Vol 70, Num 4, pp 302-310, issn 0340-6717Article

Undermethylation of Alu sequences in ICF syndrome : molecular and in situ analysisMINIOU, P; BOURC'HIS, D; MOLINA GOMES, D et al.Cytogenetics and cell genetics. 1997, Vol 77, Num 3-4, pp 308-313, issn 0301-0171Article

Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatinKOKALJ-VOKAC, N; ALMEIDA, A; VIEGAS-PEQUIGNOT, E et al.Cytogenetics and cell genetics. 1993, Vol 63, Num 1, pp 11-15, issn 0301-0171Article

Etablissement de l'empreinte parentale dans la lignée germinale = Imprinting in the germ lineKERJEAN, A; JOUVENOT, Y; VALENZA-SCHACRLY, P et al.Références en gynécologie obstétrique. 2001, Vol 8, Num 1, pp 21-27, issn 1244-8168Article

Abnormal methylation pattern in constitutive and facultive (X inactive chromosome) heterochromatin of ICF patientsMINIOU, P; JEANPIERRE, M; BLANQUET, V et al.Human molecular genetics (Print). 1994, Vol 3, Num 12, pp 2093-2102, issn 0964-6906Article

Gene for apolipoprotein CII is on human chromosome 19JEANPIERRE, M; WEIL, D; HORS-CAYLA, M. C et al.Somatic cell and molecular genetics. 1984, Vol 10, Num 6, pp 645-649, issn 0740-7750Article

Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesisKERJEAN, A; DUPONT, J.-M; VASSEUR, C et al.Human molecular genetics (Print). 2000, Vol 9, Num 14, pp 2183-2187, issn 0964-6906Article

Contribution to carrier detection and genetic counselling in X linked retinoschisisKAPLAN, J; PELET, A; HENTATI, H et al.Journal of medical genetics. 1991, Vol 28, Num 6, pp 383-388, issn 0022-2593Article

De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophyCHELLY, J; MARLHENS, F; LE MAREC, B et al.Human genetics. 1986, Vol 74, Num 2, pp 193-196, issn 0340-6717Article

Piège diagnostique et difficultés du conseil génétique dans une famille de patients porteurs de maladies neuromusculaires = Problems in the diagnosis and implications in genetic counselling for a family affected by two distinct neuromuscular disordersLESCA, G; OLLAGNON-ROMAN, E; LACHANAT, J et al.Archives de pédiatrie (Paris). 2001, Vol 8, Num 9, pp 957-960, issn 0929-693XArticle

No relationship between genetic instability in Bloom's syndrome and DNA hypomethylation of some major repetitive sequencesNOGUIEZ, P; JAULIN, C; PRAZ, F et al.Human genetics. 1993, Vol 92, Num 1, pp 57-60, issn 0340-6717Article

Duplication of HRASI, INS, AND IGF2 is not a common event in Beckwith-Wiedemann syndromeHENRY, I; JEANPIERRE, M; BARICHARD, F et al.Annales de génétique (Paris). 1988, Vol 31, Num 4, pp 216-220, issn 0003-3995Article

α-Satellite DNA methylation in normal individuals and in ICF patients : heterogeneous methylation of constitutive heterochromatin in adult and fetal tissuesMINIOU, P; JEANPIERRE, M; BOURC'HIS, D et al.Human genetics. 1997, Vol 99, Num 6, pp 738-745, issn 0340-6717Article

Molecular diagnosis of congenital bilateral absence of the vas deferens : Analyses of the CFTR gene in 64 French patientsBIENVENU, T; ADJIMAN, M; KAPLAN, J. C et al.Annales de génétique (Paris). 1997, Vol 40, Num 1, pp 5-9, issn 0003-3995Conference Paper

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinomaHENRY, I; JEANPIERRE, M; COUILLIN, P et al.Human genetics. 1989, Vol 81, Num 3, pp 273-277, issn 0340-6717Article

Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocationsBUSSON-LE CONIAT, M; SALOMON-NGUYEN, F; BERNARD, O. A et al.Leukemia. 1999, Vol 13, Num 12, pp 1975-1981, issn 0887-6924Article

Primary adhalinopathy (α-sarcoglycanopathy) : Clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyEYMARD, B; ROMERO, N. B; MERLINI, L et al.Neurology. 1997, Vol 48, Num 5, pp 1227-1234, issn 0028-3878Article