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Annales De Genetique
|
May 4, 2001
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patient
S 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 fetuses
D 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 deletion
S 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 holoprosencephaly
S Odent, B Le Marec, A Munnich, et al.
Immunology Letters
|
January 1, 1985
Cyclosporin enhances diabetes induced by low-dose streptozotocin treatment in mice
C 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.
Page
of 11
Search research articles
Search
Showing results (11-20 of 110) with videos related to
Sort By:
Page
of 11
Annales De Genetique
|
May 4, 2001
Prader-Willi syndrome and polygonosomal abnormalities in males:about a Prader-Willi/47,XYY patient
S 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 fetuses
D 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 deletion
S 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 holoprosencephaly
S Odent, B Le Marec, A Munnich, et al.
Immunology Letters
|
January 1, 1985
Cyclosporin enhances diabetes induced by low-dose streptozotocin treatment in mice
C 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.
Page
of 11