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Presse Medicale (Paris, France : 1983)|April 21, 1984
[Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency]P CouillinLa Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|January 18, 1981
[Utilization of chromosome markers and HLA antigens for prenatal identification of the male parent in artificial insemination for genetic reasons (author's transl)]J Boué, P Couillin, F YvertAnnales De Genetique|January 1, 1980
[Utilization of chromosome markers and HLA antigens for prenatal identification of the male parent in artificial insemination for genetic reasons (author's transl)]J Boué, P Couillin, F YvertHuman Genetics|February 23, 1978
Identification of the origin of triploidy by HLA markersP Couillin, J Hors, J Boué, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1986
[Antigenic study of the differentiation of the human kidney using monoclonal antibodies]J J Candelier, P Couillin, P Eydoux, et al.Pathologie-Biologie|March 1, 1976
[Permissivity of mouse-man hybrid cell clones to three enteroviruses: poliovirus II, coxsackie B3 and echovirus 11. Role of human chromosome F. 19 (author's transl)]P Couillin, A Boué, R Rebourcet, et al.Prenatal Diagnosis|July 1, 1981
Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: comparison with HLA typing in 17 pregnancies at risk for CAHM G Forest, H Bétuel, P Couillin, et al.Annales De L'Institut Pasteur. Immunology|March 1, 1987
[Determination of cell surface antigens on cryostat sections with monoclonal antibodies]J J Candelier, P Couillin, M Roturier, et al.La Nouvelle Presse Medicale|March 20, 1982
[Prenatal diagnosis of inborn errors of metabolism. 155 cases (author's transl)]J Boué, H Nicolas, C Cheruy, et al.Annales D'Endocrinologie|January 1, 1982
[Genetic of the 21 hydroxylase deficiency]A Boué, P Couillin, R Pomarède, et al.Pageof 7