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P Labrune

Showing results (101-110 of 122) with videos related to

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Prenatal Diagnosis|June 1, 1993
Antenatal thrombocytopenia in three patients with TAR (thrombocytopenia with absent radii) syndromeP Labrune, J C Pons, M Khalil, et al.
Archives Francaises De Pediatrie|October 1, 1992
[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]F Rey, V Abadie, S Lyonnet, et al.
American Journal of Medical Genetics. Part A|November 5, 2004
De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation patternG Tachdjian, A Aboura, M Benkhalifa, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 22, 2006
[Influenza vaccination coverage rate in children with underlying chronic disorders in 7 French pediatric wards]C Weil-Olivier, F Angoulvant, B Chevallier, et al.
Human Genetics|December 1, 1994
Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 casesP Labrune, A Myara, M Hadchouel, et al.
Human Genetics|February 1, 1991
Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locusM Berthelon, C Caillaud, F Rey, et al.
Human Reproduction (Oxford, England)|May 17, 2012
Are children born after infertility treatment at increased risk of retinoblastoma?L Foix-L'Hélias, I Aerts, L Marchand, et al.
Archives Francaises De Pediatrie|October 1, 1988
[Wilson's disease with liver copper in normal concentration]M Odièvre, J M Benard, H Debray, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1994
Recombinant human G-CSF (Lenograstim) for infectious complications in glycogen storage disease type Ib. Report of 7 casesJ Donadieu, B Bader-Meunier, Y Bertrand, et al.
Human Molecular Genetics|February 1, 1994
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28A Smahi, C Hyden-Granskog, B Peterlin, et al.
Pageof 13

Showing results (101-110 of 122) with videos related to

Sort By:
Pageof 13
Prenatal Diagnosis|June 1, 1993
Antenatal thrombocytopenia in three patients with TAR (thrombocytopenia with absent radii) syndromeP Labrune, J C Pons, M Khalil, et al.
Archives Francaises De Pediatrie|October 1, 1992
[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]F Rey, V Abadie, S Lyonnet, et al.
American Journal of Medical Genetics. Part A|November 5, 2004
De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation patternG Tachdjian, A Aboura, M Benkhalifa, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 22, 2006
[Influenza vaccination coverage rate in children with underlying chronic disorders in 7 French pediatric wards]C Weil-Olivier, F Angoulvant, B Chevallier, et al.
Human Genetics|December 1, 1994
Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 casesP Labrune, A Myara, M Hadchouel, et al.
Human Genetics|February 1, 1991
Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locusM Berthelon, C Caillaud, F Rey, et al.
Human Reproduction (Oxford, England)|May 17, 2012
Are children born after infertility treatment at increased risk of retinoblastoma?L Foix-L'Hélias, I Aerts, L Marchand, et al.
Archives Francaises De Pediatrie|October 1, 1988
[Wilson's disease with liver copper in normal concentration]M Odièvre, J M Benard, H Debray, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1994
Recombinant human G-CSF (Lenograstim) for infectious complications in glycogen storage disease type Ib. Report of 7 casesJ Donadieu, B Bader-Meunier, Y Bertrand, et al.
Human Molecular Genetics|February 1, 1994
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28A Smahi, C Hyden-Granskog, B Peterlin, et al.
Pageof 13