Echange sociologique et échange génétiqueSERRE J. L; LEFEVRE-WITTIER P.Population. 1977, Vol 32, Num 2, espArticle

Le droit à l'intelligence. II: Inné, acquis, donsSERRE, J.-L.Vers l'Education Nouvelle Paris. 1979, Num 338, pp 8-15Article

Mendels Rejection of the Concept of Blending InheritanceSERRE, J.-L.Fundamenta Scientiae Strasbourg. 1981, Vol 2, Num 1, pp 55-66Article

Quelle limite d'âge doit-on établir pour les donneurs de sperme ? = Wich upper age limit for semen donors?SERRE, J. L.Contraception, fertilité, sexualité (1991). 1993, Vol 21, Num 5, pp 386-387, issn 1157-8181Article

La genèse de l'oeuvre de MendelSERRE, J.-L.Recherche (La) Paris. 1984, Num 158, pp 1072-1080Article

Conditions et limites du dépistage des porteurs sains d'une mutation responsable de la mucoviscidose = Conditions and limits of carrier screening for cystic fibrosisSERRE, J. L; FEINGOLD, J.Revue d'épidémiologie et de santé publique. 1993, Vol 41, Num 5, pp 353-362, issn 0398-7620Article

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease familiesGRECO, L; BABRON, M. C; GASPARINI, P et al.Annals of human genetics. 2001, Vol 65, pp 35-41, issn 0003-4800, 1Article

A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22-q13.12CHOUERY, E; KFOURY, J; DELAGUE, V et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 4, pp 287-293, issn 1364-6745, 7 p.Article

Predicting the risk of cystic fibrosis with abnormal ultrasound signs of fetal bowel: Results of a French Molecular Collaborative Study Based on 641 Prospective CasesMULLER, F; SIMON-BOUY, B; GIRODON, E et al.American journal of medical genetics. 2002, Vol 110, Num 2, pp 109-115, issn 0148-7299Article

Analyse moléculaire de l'origine parentale de la trisomie dans deux fatries comportant deux enfants atteints de trisomie 21 libre = Molecular analysis of the parental origins of the Trisomy in two families with two regular trisomic 21 siblingsPANGALOS, C; SERRE, J. L; GHICA, M et al.Annales de génétique (Paris). 1988, Vol 31, Num 3, pp 151-154, issn 0003-3995Article

Guide to good practices to ensure privacy protection in secondary use of medical recordsRIOU, C; FRESSON, J; SERRE, J. L et al.Revue d'épidémiologie et de santé publique. 2014, Vol 62, Num 3, pp 207-214, issn 0398-7620, 8 p.Article

A polymorphis poly-A sequence in the 5' region of the aldosynthase (CYP11B2) gene may be useful in genetic diagnosis of 11β-hydroxylase genes defectsCLOT, F; JAGER, M; SIMON-BOUY, B et al.Human genetics. 1994, Vol 94, Num 3, pp 316-317, issn 0340-6717Article

Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations geneticsSERRE, J. L; SIMON-BOUY, B; MORNET, E et al.Human genetics. 1990, Vol 84, Num 5, pp 449-454, issn 0340-6717Article

Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomesOUDET, C; MORNET, E; MANDEL, J. L et al.American journal of human genetics. 1993, Vol 52, Num 2, pp 297-304, issn 0002-9297Article

Nearly 80% of cystic fibrosis heterozygotes and 64% of couples at risk may be detected through a unique screening of four mutations by ASO reverse dot blotSERRE, J. L; TAILLANDIER, A; MORNET, E et al.Genomics (San Diego, Calif.). 1991, Vol 11, Num 4, pp 1149-1151, issn 0888-7543Article

Polymorphism and genetic evolution in an isolate in the Antilles: Saint-BarthélémySERRE, J. L; BABRON, M.-C.Annals of human biology. 1985, Vol 12, Num 5, pp 413-419, issn 0301-4460Article

A new mechanism of dominance in hypophosphatasia : the mutated protein can disturb the cell localization of the wild-type proteinLIA-BALDINI, A. S; BRUN-HEATH, I; CARRION, C et al.Human genetics. 2008, Vol 123, Num 4, pp 429-432, issn 0340-6717, 4 p.Article

Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesMORNET, E; SIMON-BOUY, B; SERRE, J. L et al.Clinical genetics. 1989, Vol 35, Num 2, pp 81-87, issn 0009-9163Article

Genetic differences between cystic fibrosis with and without meconium ileusMORNET, E; SIMON-BOUY, B; SERRE, J. L et al.Lancet (British edition). 1988, Num 8582, pp 376-378, issn 0140-6736Article

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

Some trends in medical populations geneticsFEINGOLD, J; SERRE, J. L; CARNEVALE, P et al.Experientia. 1986, Vol 42, Num 10, pp 1102-1109, issn 0014-4754Article

The intermediate alleles of the fragile X CGG repeat in patients with mental retardationMORNET, E; CHATEAU, C; SIMON-BOUY, B et al.Clinical genetics. 1998, Vol 53, Num 3, pp 200-201, issn 0009-9163Article

Analyse des systèmes de marqueurs érythrocytaires dans la population vietnamienneTRAN, M.-H; SERRE, J.-L; LEPLUS, R et al.Anthropologie (L') Paris. 1980, Vol 84, Num 1, pp 119-125Article

Molecular analysis of a reciprocal translocation t(5;11)(q11;p13) in a WAGR patientPUISSANT, H; AZOULAY, M; SERRE, J.-L et al.Human genetics. 1988, Vol 79, Num 3, pp 280-282, issn 0340-6717Article

Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndromeMORNET, E; CHATEAU, C; TAILLANDIER, A et al.Human genetics. 1996, Vol 97, Num 4, pp 512-515, issn 0340-6717Article