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M C Vinet

Showing results (1-10 of 22) with videos related to

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Prenatal Diagnosis|April 1, 1983
Amniotic fluid protease activity and the prenatal detection of cystic fibrosisL Poenaru, M C Vinet
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 25, 1981
Human amniotic fluid alpha-glucosidaseL Poenaru, M C Vinet, J C Dreyfus
Human Genetics|August 1, 1989
Autosomal dominant polycystic kidney disease and alpha -4.2 thalassemia in a Caucasian familyM C Vinet, C Dodé, O Pascal, et al.
Clinical Genetics|December 1, 1979
Antenatal diagnosis in three pregnancies at risk for mannosidosisL Poenaru, S Girard, F Thepot, et al.
Human Genetics|July 1, 1990
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locusL Bachner, M C Vinet, R Lacave, et al.
Molecular and Cellular Neurosciences|October 10, 2001
Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous systemG Friocourt, P Chafey, P Billuart, et al.
Journal of Medical Genetics|April 1, 1994
Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.
American Journal of Human Genetics|April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.
American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.
Pathologie-Biologie|January 14, 1999
Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|April 1, 1983
Amniotic fluid protease activity and the prenatal detection of cystic fibrosisL Poenaru, M C Vinet
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 25, 1981
Human amniotic fluid alpha-glucosidaseL Poenaru, M C Vinet, J C Dreyfus
Human Genetics|August 1, 1989
Autosomal dominant polycystic kidney disease and alpha -4.2 thalassemia in a Caucasian familyM C Vinet, C Dodé, O Pascal, et al.
Clinical Genetics|December 1, 1979
Antenatal diagnosis in three pregnancies at risk for mannosidosisL Poenaru, S Girard, F Thepot, et al.
Human Genetics|July 1, 1990
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locusL Bachner, M C Vinet, R Lacave, et al.
Molecular and Cellular Neurosciences|October 10, 2001
Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous systemG Friocourt, P Chafey, P Billuart, et al.
Journal of Medical Genetics|April 1, 1994
Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.
American Journal of Human Genetics|April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.
American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.
Pathologie-Biologie|January 14, 1999
Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, et al.
Pageof 3