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G Viot

Showing results (21-30 of 49) with videos related to

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Nouvelle Revue Francaise D'Hematologie|January 1, 1984
[Contesting a critique of the comparison of 2 prognostic classifications of multiple myeloma]A Pesce, J P Cassuto, C Grisot, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 22, 2007
First-trimester ultrasound diagnosis of skeletal dysplasia associated with increased nuchal translucency thicknessC Ngo, G Viot, M C Aubry, et al.
Journal of Immunological Methods|January 1, 1980
A sandwich method of enzyme immunoassay. III. Assay for human beta-2 microglobulin compared with radioimmunoassayB Ferrua, C Vincent, J P Revillard, et al.
Pathologie-Biologie|September 1, 1978
[Determination of beta2-microglobulin in breast, lung, colorectal and ENT carcinoma (author's transl)]G Viot, M Leca, J L Moll, et al.
Pathologie-Biologie|September 1, 1978
beta2-Microglobulin in lymphoproliferative disorders with special reference to gammapathiesJ P Cassuto, B P Krebs, M V Joyner, et al.
Prenatal Diagnosis|January 21, 2003
Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygromaE Pannier, G Viot, M C Aubry, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 15, 2002
Prenatal diagnosis of fetal tail and postabortum anatomical descriptionG Grangé, J Tantau, E Pannier, et al.
American Journal of Medical Genetics|April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicismL Faivre, G Viot, M Prieur, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1R Dufourcq-Lagelouse, N Lambert, M Duval, et al.
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Nouvelle Revue Francaise D'Hematologie|January 1, 1984
[Contesting a critique of the comparison of 2 prognostic classifications of multiple myeloma]A Pesce, J P Cassuto, C Grisot, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 22, 2007
First-trimester ultrasound diagnosis of skeletal dysplasia associated with increased nuchal translucency thicknessC Ngo, G Viot, M C Aubry, et al.
Journal of Immunological Methods|January 1, 1980
A sandwich method of enzyme immunoassay. III. Assay for human beta-2 microglobulin compared with radioimmunoassayB Ferrua, C Vincent, J P Revillard, et al.
Pathologie-Biologie|September 1, 1978
[Determination of beta2-microglobulin in breast, lung, colorectal and ENT carcinoma (author's transl)]G Viot, M Leca, J L Moll, et al.
Pathologie-Biologie|September 1, 1978
beta2-Microglobulin in lymphoproliferative disorders with special reference to gammapathiesJ P Cassuto, B P Krebs, M V Joyner, et al.
Prenatal Diagnosis|January 21, 2003
Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygromaE Pannier, G Viot, M C Aubry, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 15, 2002
Prenatal diagnosis of fetal tail and postabortum anatomical descriptionG Grangé, J Tantau, E Pannier, et al.
American Journal of Medical Genetics|April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicismL Faivre, G Viot, M Prieur, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1R Dufourcq-Lagelouse, N Lambert, M Duval, et al.
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Pageof 5