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Maladies démyélinisantes d'origine génétique : Maladies démyélinisantes du système nerveux central = Genetic demyelinating diseases : Central nervous system demyelinating diseasesLABAUGE, Pierre; BOESPFLUG-TANGUY, Odile.La Presse médicale (1983). 2010, Vol 39, Num 3, pp 363-370, issn 0755-4982, 8 p.Article

Maladies génétiques = Genetic diseasesMS. Médecine sciences. 2005, Vol 21, Num 11, issn 0767-0974, 111 p.Serial Issue

Discovery of a novel Torque teno sus virus species: genetic characterization, epidemiological assessment and disease associationCORNELISSEN-KEIJSERS, Vivian; JIMENEZ-MELSIO, Alexandra; SONNEMANS, Denny et al.Journal of general virology. 2012, Vol 93, pp 2682-2691, issn 0022-1317, 10 p., 12Article

Genetics of neurodegenerative diseases: insights from high-throughput resequencingTSUJI, Shoji.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R65-R70, NSArticle

Bone marrow replacement in the treatment of hemolytic disease in miceBERNSTEIN, S. E; DEVEAU, S. A.Experimental hematology. 1989, Vol 17, Num 10, pp 0004-1010, issn 0301-472X, 1007 p.Article

Autosomal dominant congenital cataract on chromosome 16MARNER, E.Clinical genetics. 1989, Vol 36, Num 5, issn 0009-9163, p. 326Conference Paper

Towards a complete resolution of the genetic architecture of diseaseSINGLETON, Andrew B; HARDY, John; TRAYNOR, Bryan J et al.Trends in genetics (Regular ed.). 2010, Vol 26, Num 10, pp 438-442, issn 0168-9525, 5 p.Article

Effectiveness of prevention of cystic fibrosis by artificial insemination by donor can be markedly improved by DNA-analysis of sperm donorsTEN KATE, L. P; TE MEERMAN, G. J; BUYS, C. H. C. M et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 148-149, issn 0148-7299, 2 p.Article

Benign familial hematuriaYOSHIKAWA, N; MATSUYAMA, S; IIJIMA, K et al.Archives of pathology & laboratory medicine (1976). 1988, Vol 112, Num 8, pp 794-797, issn 0363-0153Article

Heritable disorders of hairBIRNBAUM, P. S; BADEN, H. P.Dermatologic clinics. 1987, Vol 5, Num 1, pp 137-153, issn 0733-8635Article

Recent research developments in human genetics (Volume 2, 2004)Pandalai, S. G.Recent research developments in human genetics. 2004, isbn 81-7736-212-7, 223 p., isbn 81-7736-212-7Book

Heritable nail disordersKUCIRKA, S. J; SCHER, R. K.Dermatologic clinics. 1987, Vol 5, Num 1, pp 179-191, issn 0733-8635Article

The expanding clinical and genetic spectrum of ATP1A3-related disordersROSEWICH, Hendrik; OHLENBUSCH, Andreas; GÄRTNER, Jutta et al.Neurology. 2014, Vol 82, Num 11, pp 945-955, issn 0028-3878, 11 p.Article

Functional modules, mutational load and human genetic diseaseZAGHLOUL, Norann A; KATSANIS, Nicholas.Trends in genetics (Regular ed.). 2010, Vol 26, Num 4, pp 168-176, issn 0168-9525, 9 p.Article

Nuclear genes and mitochondrial translation: a new class of genetic diseaseJACOBS, Howard T; TURNBULL, Douglass M.Trends in genetics (Regular ed.). 2005, Vol 21, Num 6, pp 312-314, issn 0168-9525, 3 p.Article

Genetics for Pediatricians-II. SymposiumIndian journal of pediatrics. 2000, Vol 67, Num 12, pp 893-928, issn 0019-5456, 33 p.Conference Proceedings

Issues in genetic testing. Annual forumClinical chemistry (Baltimore, Md.). 1999, Vol 45, Num 5, pp 725-749, issn 0009-9147Conference Proceedings

The American Society of Human Genetics ASHG. Annual MeetingAmerican journal of human genetics. 1998, Vol 63, Num 4, issn 0002-9297, 653 p.Conference Proceedings

Online Mendelian Inheritance in ManRASHBASS, J.Trends in genetics (Regular ed.). 1995, Vol 11, Num 7, issn 0168-9525, p. 291Article

American Society of Human Genetics ASHG. Annual meetingAmerican journal of human genetics. 1995, Vol 57, Num 4, issn 0002-9297, 545 p., SUPConference Proceedings

British medical genetics conferenceJournal of medical genetics. 1994, Vol 31, Num 2, pp 162-175, issn 0022-2593Conference Proceedings

26th annual meeting of the European Society of Human Genetics (abstracts, Paris, June 2-5, 1994)European Society of Human Genetics. Annual meeting. 1994, 160 p.Conference Proceedings

Syndrome des cheveux incoiffables, familial = Uncombable hair syndrome: familial occurrenceJELEN, G.Les Nouvelles dermatologiques. 1988, Vol 7, Num 1, pp 64-66, issn 0752-5370Article

Incontinentia pigmenti: a longitudinal studyÓBRIEN, J. E; FEINGOLD, M.American journal of diseases of children (1960). 1985, Vol 139, Num 7, pp 711-712, issn 0002-922XArticle

Passé et avenir de la crénothérapie en gynécologie à Luxeuil-les-bainsAUBRY, R; WAHL, P.1985, 111 p.Thesis

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