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H Plauchu

Showing results (41-50 of 116) with videos related to

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Pediatrie|January 1, 1987
[WAGR syndrome, Wilms' tumor, aniridia, gonadoblastoma, mental retardation: a review apropos of 2 cases]M C Mochon, J F Blanc, H Plauchu, et al.
Gastroenterology|August 1, 1993
Hepatic involvement in hereditary hemorrhagic telangiectasia: clinical, radiological, and hemodynamic studies of 11 casesG Bernard, F Mion, L Henry, et al.
Prenatal Diagnosis|July 1, 1991
Duplication of chromosome 11 centromere in fetal and maternal karyotypes: a new variant?M Till, A Rafat, C Charrin, et al.
La Nouvelle Presse Medicale|April 21, 1979
[Systematic neonatal screening for Duchenne muscular dystrophy]C Dellamonica, J M Robert, J Cotte, et al.
Journal of Medical Genetics|December 1, 1998
Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosisS Pinson, J Yaouanq, A M Jouanolle, et al.
American Journal of Medical Genetics|March 1, 1989
Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited populationH Plauchu, J P de Chadarévian, A Bideau, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|July 1, 1985
[Sampling of chorionic villi during the first trimester of pregnancy]R C Rudigoz, D Germain, N Philippe, et al.
Journal of Internal Medicine|June 19, 2013
Immunological abnormalities associated with hereditary haemorrhagic telangiectasiaA Guilhem, C Malcus, B Clarivet, et al.
Annales De Genetique|January 1, 1988
[The 48,XXXX syndrome: study of psychomotor development from birth to 11 years of age and review of the literature]H Plauchu, E Ollagnon-Roman, J P Armand, et al.
Journal De Genetique Humaine|June 1, 1984
[Case of megadolichoureter due to an anomaly of the ureterovesical junction in 2 brothers]H Plauchu, H Dodat, B Betend, et al.
Pageof 12

Showing results (41-50 of 116) with videos related to

Sort By:
Pageof 12
Pediatrie|January 1, 1987
[WAGR syndrome, Wilms' tumor, aniridia, gonadoblastoma, mental retardation: a review apropos of 2 cases]M C Mochon, J F Blanc, H Plauchu, et al.
Gastroenterology|August 1, 1993
Hepatic involvement in hereditary hemorrhagic telangiectasia: clinical, radiological, and hemodynamic studies of 11 casesG Bernard, F Mion, L Henry, et al.
Prenatal Diagnosis|July 1, 1991
Duplication of chromosome 11 centromere in fetal and maternal karyotypes: a new variant?M Till, A Rafat, C Charrin, et al.
La Nouvelle Presse Medicale|April 21, 1979
[Systematic neonatal screening for Duchenne muscular dystrophy]C Dellamonica, J M Robert, J Cotte, et al.
Journal of Medical Genetics|December 1, 1998
Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosisS Pinson, J Yaouanq, A M Jouanolle, et al.
American Journal of Medical Genetics|March 1, 1989
Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited populationH Plauchu, J P de Chadarévian, A Bideau, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|July 1, 1985
[Sampling of chorionic villi during the first trimester of pregnancy]R C Rudigoz, D Germain, N Philippe, et al.
Journal of Internal Medicine|June 19, 2013
Immunological abnormalities associated with hereditary haemorrhagic telangiectasiaA Guilhem, C Malcus, B Clarivet, et al.
Annales De Genetique|January 1, 1988
[The 48,XXXX syndrome: study of psychomotor development from birth to 11 years of age and review of the literature]H Plauchu, E Ollagnon-Roman, J P Armand, et al.
Journal De Genetique Humaine|June 1, 1984
[Case of megadolichoureter due to an anomaly of the ureterovesical junction in 2 brothers]H Plauchu, H Dodat, B Betend, et al.
Pageof 12