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Journal De Genetique Humaine|December 1, 1989
[Genetic mapping of chromosome X: known localizations]C Verellen-DumoulinJournal De Genetique Humaine|January 1, 1989
[Psychological implications of family studies by molecular biology. An example--muscular dystrophy]J Y Hayez, C Verellen-DumoulinAnnales De Chirurgie De La Main Et Du Membre Superieur : Organe Officiel Des Societes De Chirurgie De La Main = Annals of Hand and Upper Limb Surgery|January 1, 1992
[Trismus-pseudocamptodactyly syndrome: presentation and genealogy of a new European case]J J Rombouts, C Verellen-DumoulinComptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1985
[Mutagen sensitivity and the repair process of the lymphocytes in the Werner syndrome]G Deknudt, C Verellen-Dumoulin, A LéonardActa Clinica Belgica|December 7, 2010
Chorea associated with anti-phospholipid antibodies: case reportJ Demonty, M Gonce, P Ribai, et al.Acta Neurologica Belgica|January 25, 2020
Hereditary axonal neuropathy related to MME gene mutation in a family with fetomaternal alloimmune glomerulonephritisM Dupuis, J M Raymackers, N Ackermans, et al.Journal of Medical Genetics|November 1, 1994
High CTG repeat number in nodular thyroid tissue from a myotonic dystrophy patientC Daumerie, N Lannoy, J P Squifflet, et al.American Journal of Medical Genetics|May 15, 1993
Oral-facial-digital syndrome type I in a newborn maleY Gillerot, M Heimann, C Fourneau, et al.The Journal of Pediatrics|November 5, 1997
Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt managementT Sluysmans, D Tuerlinckx, C Hubinont, et al.Prenatal Diagnosis|July 1, 1984
S-100 protein in amniotic fluid of anencephalic fetusesC J Sindic, M Freund, N Van Regemorter, et al.Pageof 5