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Journal De Genetique Humaine|June 1, 1979
[Heterozygote detection in phenylketonuria by means of an oral load of phenylalanine]J L Dhondt, J P FarriauxJournal De Genetique Humaine|January 1, 1989
[Argininosuccinic aciduria. A new case revealed by psychiatric disorders]S Odent, M Roussey, H Journel, et al.Journal De Genetique Humaine|January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]P Mujica, B Leheup, S Gilgenkrantz, et al.Journal De Genetique Humaine|December 1, 1989
[Diagnosis of deficiency in cofactor of phenylalanine hydroxylase: a metabolic emergency]M Meyer, G Malpuech, J Geneste, et al.Journal De Genetique Humaine|December 1, 1989
[Conradi-H:unermann chondrodysplasia punctata and fetal alcoholism]P Sarda, S Guillaumont, J Jalaguier, et al.Journal De Genetique Humaine|December 1, 1989
[F.G. syndrome: a rare and/or extremely polymorphic syndrome?]P Sarda, G Lefort, J Jalaguier, et al.Journal De Genetique Humaine|December 1, 1989
[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis]C Ferec, C Verlingue, P ParentJournal De Genetique Humaine|December 1, 1989
[Genetic mapping of chromosome X: known localizations]C Verellen-DumoulinJournal De Genetique Humaine|August 1, 1988
[Otologic signs and early diagnosis of Turner syndrome. Reevaluation of 30 cases]B P Leheup, P Perrin, C Perrin, et al.Journal De Genetique Humaine|June 1, 1988
[Bourneville's tuberous sclerosis and genetic counseling. Study of 36 families]A David, M L BriardPageof 47