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P Labrune

Showing results (71-80 of 122) with videos related to

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Annales De Biologie Clinique|February 15, 2001
[Refinement and role of the diagnosis of Gilbert disease with molecular biology]B Le Bihan-Levaufre, J Francoual, P Labrune, et al.
Prenatal Diagnosis|July 17, 1998
Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestionP Trioche, J Francoual, F Audibert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 26, 2010
[Primary paraesophageal hiatal hernia]M Cochez, K Milcent, A Isapof, et al.
Acta Paediatrica Scandinavica|September 1, 1989
Human immunodeficiency virus-associated thrombocytopenia in infantsP Labrune, S Blanche, N Catherine, et al.
Archives of Disease in Childhood|September 18, 1999
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndromeP Trioche, J Chalas, J Francoual, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1992
Bilirubin uridine diphosphate glucuronosyltransferase hepatic activity in jaundice associated with congenital hypothyroidismP Labrune, A Myara, P Huguet, et al.
American Journal of Medical Genetics|December 31, 1997
Severe brain and limb defects with possible autosomal recessive inheritance: a series of six cases and review of the literatureP Labrune, P Trioche, C Fallet-Bianco, et al.
Archives Francaises De Pediatrie|August 1, 1989
[Problems stemming from pregnancy in a woman with phenylketonuria]P Labrune, C Brunet, F Rey, et al.
Clinical Genetics|November 4, 2004
Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 casesF M Petit, V Gajdos, J Francoual, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|December 2, 2005
[Cocaine and trisomy 8 associated with prenatal diagnosis of corpus callosum agenesis]E Gonzales, L Caeymaex, A Aboura, et al.
Pageof 13

Showing results (71-80 of 122) with videos related to

Sort By:
Pageof 13
Annales De Biologie Clinique|February 15, 2001
[Refinement and role of the diagnosis of Gilbert disease with molecular biology]B Le Bihan-Levaufre, J Francoual, P Labrune, et al.
Prenatal Diagnosis|July 17, 1998
Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestionP Trioche, J Francoual, F Audibert, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 26, 2010
[Primary paraesophageal hiatal hernia]M Cochez, K Milcent, A Isapof, et al.
Acta Paediatrica Scandinavica|September 1, 1989
Human immunodeficiency virus-associated thrombocytopenia in infantsP Labrune, S Blanche, N Catherine, et al.
Archives of Disease in Childhood|September 18, 1999
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndromeP Trioche, J Chalas, J Francoual, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1992
Bilirubin uridine diphosphate glucuronosyltransferase hepatic activity in jaundice associated with congenital hypothyroidismP Labrune, A Myara, P Huguet, et al.
American Journal of Medical Genetics|December 31, 1997
Severe brain and limb defects with possible autosomal recessive inheritance: a series of six cases and review of the literatureP Labrune, P Trioche, C Fallet-Bianco, et al.
Archives Francaises De Pediatrie|August 1, 1989
[Problems stemming from pregnancy in a woman with phenylketonuria]P Labrune, C Brunet, F Rey, et al.
Clinical Genetics|November 4, 2004
Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 casesF M Petit, V Gajdos, J Francoual, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|December 2, 2005
[Cocaine and trisomy 8 associated with prenatal diagnosis of corpus callosum agenesis]E Gonzales, L Caeymaex, A Aboura, et al.
Pageof 13