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P Burlet

Showing results (11-20 of 32) with videos related to

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Lancet (London, England)|August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy InvestigatorsJ Melki, P Sheth, S Abdelhak, et al.
Gynecologie, Obstetrique & Fertilite|September 6, 2005
[Extending preimplantation genetic diagnosis to HLA typing: the Paris experience]J Steffann, N Frydman, P Burlet, et al.
Cell|January 13, 1995
Identification and characterization of a spinal muscular atrophy-determining geneS Lefebvre, L Bürglen, S Reboullet, et al.
Reproductive Biomedicine Online|February 7, 2008
Preimplantation genetic diagnosis for autosomal recessive polycystic kidney diseaseN Gigarel, N Frydman, P Burlet, et al.
American Journal of Human Genetics|January 1, 1997
The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann diseaseL Bürglen, T Seroz, P Miniou, et al.
Clinical Genetics|March 8, 2013
Successful pre-implantation genetic diagnosis for Hirschsprung diseaseP Burlet, C Steichen, L Hesters, et al.
Genomics|March 1, 1993
Refined linkage map of chromosome 5 in the region of the spinal muscular atrophy geneJ Melki, P Burlet, O Clermont, et al.
Genomics|June 1, 1994
Genetic linkage studies of Machado-Joseph disease with chromosome 14q STRPs in 16 Portuguese-Azorean kindredsJ Sequeiros, I Silveira, P Maciel, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies]J Melki, S Lefebvre, L Burglen, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probesJ Melki, S Abdelhak, P Burlet, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Lancet (London, England)|August 4, 1990
Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy InvestigatorsJ Melki, P Sheth, S Abdelhak, et al.
Gynecologie, Obstetrique & Fertilite|September 6, 2005
[Extending preimplantation genetic diagnosis to HLA typing: the Paris experience]J Steffann, N Frydman, P Burlet, et al.
Cell|January 13, 1995
Identification and characterization of a spinal muscular atrophy-determining geneS Lefebvre, L Bürglen, S Reboullet, et al.
Reproductive Biomedicine Online|February 7, 2008
Preimplantation genetic diagnosis for autosomal recessive polycystic kidney diseaseN Gigarel, N Frydman, P Burlet, et al.
American Journal of Human Genetics|January 1, 1997
The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann diseaseL Bürglen, T Seroz, P Miniou, et al.
Clinical Genetics|March 8, 2013
Successful pre-implantation genetic diagnosis for Hirschsprung diseaseP Burlet, C Steichen, L Hesters, et al.
Genomics|March 1, 1993
Refined linkage map of chromosome 5 in the region of the spinal muscular atrophy geneJ Melki, P Burlet, O Clermont, et al.
Genomics|June 1, 1994
Genetic linkage studies of Machado-Joseph disease with chromosome 14q STRPs in 16 Portuguese-Azorean kindredsJ Sequeiros, I Silveira, P Maciel, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies]J Melki, S Lefebvre, L Burglen, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probesJ Melki, S Abdelhak, P Burlet, et al.
Pageof 4