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J F Mattei

Showing results (181-190 of 202) with videos related to

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Human Genetics|April 1, 1986
The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosomeM G Mattei, P M Alliel, A Dautigny, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
Gynecologie, Obstetrique & Fertilite|March 26, 2011
[Decision-making in termination of pregnancy: a French perspective]G Gorincour, S Tassy, A Payot, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian populationC Badens, F Martinez di Montemuros, I Thuret, et al.
Clinical Rheumatology|August 15, 2000
A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjögren's syndrome: a preliminary reportB Granel, V Ravix, K Pedeillier, et al.
Journal of Medical Genetics|July 29, 1999
Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counsellingA Moncla, P Malzac, M O Livet, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
Human Genetics|April 1, 1989
Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridizationM G Mattei, J P Périn, P M Alliel, et al.
Presse Medicale (Paris, France : 1983)|February 3, 1996
[Genetic hemoglobin diseases. Prevention at centers for family planning and education of maternal-child protection in Marseille]D Lena-Russo, N Erny, F Serradimigni, et al.
Pageof 21

Showing results (181-190 of 202) with videos related to

Sort By:
Pageof 21
Human Genetics|April 1, 1986
The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosomeM G Mattei, P M Alliel, A Dautigny, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
Gynecologie, Obstetrique & Fertilite|March 26, 2011
[Decision-making in termination of pregnancy: a French perspective]G Gorincour, S Tassy, A Payot, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian populationC Badens, F Martinez di Montemuros, I Thuret, et al.
Clinical Rheumatology|August 15, 2000
A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjögren's syndrome: a preliminary reportB Granel, V Ravix, K Pedeillier, et al.
Journal of Medical Genetics|July 29, 1999
Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counsellingA Moncla, P Malzac, M O Livet, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
Human Genetics|April 1, 1989
Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridizationM G Mattei, J P Périn, P M Alliel, et al.
Presse Medicale (Paris, France : 1983)|February 3, 1996
[Genetic hemoglobin diseases. Prevention at centers for family planning and education of maternal-child protection in Marseille]D Lena-Russo, N Erny, F Serradimigni, et al.
Pageof 21