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J C Lambert

Showing results (31-40 of 112) with videos related to

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Bulletin Des Societes D'Ophtalmologie De France|February 1, 1984
[Histiocytosis X with neurologic syndrome. Treatment of a case with Velbe]F Lods, R Mariani, A Deville, et al.
Neuroscience Letters|December 3, 2002
No association of the HLA-A2 allele with Alzheimer's diseaseL Araria-Goumidi, J C Lambert, D Cottel, et al.
Journal of Medical Genetics|May 1, 1990
Branchial dysplasia, mental deficiency, club feet, and inguinal herniae: a report of two further cases associated with paucity of interlobular bile ductsJ C Lambert, M C Saint-Paul, F Bastiani, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1986
[Effect of alpha-fetoprotein on isolated mouse oocytes]J C Lambert, G Vallette, G E Seralini, et al.
Pediatrie|April 1, 1985
[The Vater association in a newborn infant of a diabetic mother]P Boutte, J S Valla, J C Lambert, et al.
Lancet (London, England)|June 1, 1996
Presenilin-1 polymorphism and Alzheimer's disease. The Alzheimer's Study GroupJ Pérez-Tur, F Wavrant-De Vrieze, J C Lambert, et al.
Archives Francaises De Pediatrie|May 1, 1983
[Association of hereditary hydrocephalus and holoprosencephaly]J C Lambert, M Ferrari, M Donzeau, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|January 1, 1986
Effects of alphafetoprotein on isolated mouse oocytesJ C Lambert, G E Seralini, C Stora, et al.
Human Molecular Genetics|April 18, 1998
A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's diseaseJ C Lambert, F Pasquier, D Cottel, et al.
Journal of Medical Genetics|August 28, 1999
Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromesA David, P Bitoun, D Lacombe, et al.
Pageof 12

Showing results (31-40 of 112) with videos related to

Sort By:
Pageof 12
Bulletin Des Societes D'Ophtalmologie De France|February 1, 1984
[Histiocytosis X with neurologic syndrome. Treatment of a case with Velbe]F Lods, R Mariani, A Deville, et al.
Neuroscience Letters|December 3, 2002
No association of the HLA-A2 allele with Alzheimer's diseaseL Araria-Goumidi, J C Lambert, D Cottel, et al.
Journal of Medical Genetics|May 1, 1990
Branchial dysplasia, mental deficiency, club feet, and inguinal herniae: a report of two further cases associated with paucity of interlobular bile ductsJ C Lambert, M C Saint-Paul, F Bastiani, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1986
[Effect of alpha-fetoprotein on isolated mouse oocytes]J C Lambert, G Vallette, G E Seralini, et al.
Pediatrie|April 1, 1985
[The Vater association in a newborn infant of a diabetic mother]P Boutte, J S Valla, J C Lambert, et al.
Lancet (London, England)|June 1, 1996
Presenilin-1 polymorphism and Alzheimer's disease. The Alzheimer's Study GroupJ Pérez-Tur, F Wavrant-De Vrieze, J C Lambert, et al.
Archives Francaises De Pediatrie|May 1, 1983
[Association of hereditary hydrocephalus and holoprosencephaly]J C Lambert, M Ferrari, M Donzeau, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|January 1, 1986
Effects of alphafetoprotein on isolated mouse oocytesJ C Lambert, G E Seralini, C Stora, et al.
Human Molecular Genetics|April 18, 1998
A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's diseaseJ C Lambert, F Pasquier, D Cottel, et al.
Journal of Medical Genetics|August 28, 1999
Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromesA David, P Bitoun, D Lacombe, et al.
Pageof 12