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S Odent

Showing results (11-20 of 110) with videos related to

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Annales De Genetique|May 4, 2001
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patientS Odent, S Taque, J Lucas, et al.
American Journal of Medical Genetics|May 26, 1999
Heterotaxy-neural tube defect and holoprosencephaly occuring independently in two sib fetusesD Bonneau, M Maréchaud, S Odent, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2008
[Syndromic mental retardation]S Odent, L Pasquier, C de la Rochebrochard, et al.
Annales De Pediatrie|April 1, 1988
[Aortic thrombosis manifested by a picture of aortic coarctation: a complication of neonatal umbilical catheterization]I Casadevall, P Bétrémieux, P Pladys, et al.
Journal De Genetique Humaine|September 1, 1989
[A family with x-linked hydrocephaly followed for 20 years: echographic prenatal diagnosis; elective abortion]B Le Marec, J Milon, S Odent, et al.
Ophthalmic Genetics|April 21, 2016
Posterior amorphous corneal dystrophy caused by a de novo deletionS Odent, I Casteels, C Cassiman, et al.
Pediatrie|January 1, 1988
[Hyperosmolar coma in a premature newborn infant: iatrogenic complication of parenteral feeding]I Casadevall, P Betremieux, P Pladys, et al.
American Journal of Medical Genetics|May 30, 1998
Segregation analysis in nonsyndromic holoprosencephalyS Odent, B Le Marec, A Munnich, et al.
Immunology Letters|January 1, 1985
Cyclosporin enhances diabetes induced by low-dose streptozotocin treatment in miceC Sestier, S Odent-Pogu, M Bonneville, et al.
Journal De Genetique Humaine|January 1, 1989
[Argininosuccinic aciduria. A new case revealed by psychiatric disorders]S Odent, M Roussey, H Journel, et al.
Pageof 11

Showing results (11-20 of 110) with videos related to

Sort By:
Pageof 11
Annales De Genetique|May 4, 2001
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patientS Odent, S Taque, J Lucas, et al.
American Journal of Medical Genetics|May 26, 1999
Heterotaxy-neural tube defect and holoprosencephaly occuring independently in two sib fetusesD Bonneau, M Maréchaud, S Odent, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2008
[Syndromic mental retardation]S Odent, L Pasquier, C de la Rochebrochard, et al.
Annales De Pediatrie|April 1, 1988
[Aortic thrombosis manifested by a picture of aortic coarctation: a complication of neonatal umbilical catheterization]I Casadevall, P Bétrémieux, P Pladys, et al.
Journal De Genetique Humaine|September 1, 1989
[A family with x-linked hydrocephaly followed for 20 years: echographic prenatal diagnosis; elective abortion]B Le Marec, J Milon, S Odent, et al.
Ophthalmic Genetics|April 21, 2016
Posterior amorphous corneal dystrophy caused by a de novo deletionS Odent, I Casteels, C Cassiman, et al.
Pediatrie|January 1, 1988
[Hyperosmolar coma in a premature newborn infant: iatrogenic complication of parenteral feeding]I Casadevall, P Betremieux, P Pladys, et al.
American Journal of Medical Genetics|May 30, 1998
Segregation analysis in nonsyndromic holoprosencephalyS Odent, B Le Marec, A Munnich, et al.
Immunology Letters|January 1, 1985
Cyclosporin enhances diabetes induced by low-dose streptozotocin treatment in miceC Sestier, S Odent-Pogu, M Bonneville, et al.
Journal De Genetique Humaine|January 1, 1989
[Argininosuccinic aciduria. A new case revealed by psychiatric disorders]S Odent, M Roussey, H Journel, et al.
Pageof 11