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G Lesca

Showing results (1-10 of 41) with videos related to

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Revue Neurologique|May 25, 2015
Epilepsy genetics: the ongoing revolutionG Lesca, C Depienne
Neurology|November 13, 2002
Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxiasC Goizet, G Lesca, A Dürr, et al.
Journal of Medical Genetics|July 13, 2002
Predictive testing in the context of pregnancy: experience in Huntington's disease and autosomal dominant cerebellar ataxiaG Lesca, C Goizet, A Dürr
Revue Neurologique|April 6, 2013
[Family impact of FXTAS diagnosis: genetic counseling for at-risk relatives]G Lesca, S Lejeune, D Hernette, et al.
Journal of the Neurological Sciences|March 5, 2011
A novel exon 3 mutation in a Tunisian patient with Lafora's diseaseH Mrabet Khiari, G Lesca, A Malafosse, et al.
Journal of Neurology|January 21, 2003
Acute myelitis in early Borrelia burgdorferi infectionG Lesca, R Deschamps, C Lubetzki, et al.
Genetic Counseling (Geneva, Switzerland)|April 23, 2005
Unusual clinical syndrome in a boy with 45,X/46,XY mosaicismJ Lespinasse, S Murthy, G Lesca, et al.
Prenatal Diagnosis|April 21, 1999
Trisomy 17 mosaicism in amniotic fluid cells not found at birth in blood but present in skin fibroblastsG Lesca, D Boggio, V Bellec, et al.
Clinical Genetics|March 1, 2005
Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardationG Lesca, Om Sinilnikova, G Theuil, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 8, 2023
Prenatal diagnosis of microcephaly with simplified gyral pattern: series of eight casesS Cabet, A Putoux, G Lesca, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Revue Neurologique|May 25, 2015
Epilepsy genetics: the ongoing revolutionG Lesca, C Depienne
Neurology|November 13, 2002
Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxiasC Goizet, G Lesca, A Dürr, et al.
Journal of Medical Genetics|July 13, 2002
Predictive testing in the context of pregnancy: experience in Huntington's disease and autosomal dominant cerebellar ataxiaG Lesca, C Goizet, A Dürr
Revue Neurologique|April 6, 2013
[Family impact of FXTAS diagnosis: genetic counseling for at-risk relatives]G Lesca, S Lejeune, D Hernette, et al.
Journal of the Neurological Sciences|March 5, 2011
A novel exon 3 mutation in a Tunisian patient with Lafora's diseaseH Mrabet Khiari, G Lesca, A Malafosse, et al.
Journal of Neurology|January 21, 2003
Acute myelitis in early Borrelia burgdorferi infectionG Lesca, R Deschamps, C Lubetzki, et al.
Genetic Counseling (Geneva, Switzerland)|April 23, 2005
Unusual clinical syndrome in a boy with 45,X/46,XY mosaicismJ Lespinasse, S Murthy, G Lesca, et al.
Prenatal Diagnosis|April 21, 1999
Trisomy 17 mosaicism in amniotic fluid cells not found at birth in blood but present in skin fibroblastsG Lesca, D Boggio, V Bellec, et al.
Clinical Genetics|March 1, 2005
Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardationG Lesca, Om Sinilnikova, G Theuil, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 8, 2023
Prenatal diagnosis of microcephaly with simplified gyral pattern: series of eight casesS Cabet, A Putoux, G Lesca, et al.
Pageof 5