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N Morichon

Showing results (21-30 of 31) with videos related to

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Lancet (London, England)|January 22, 1994
SRY-negative XX fetus with complete male phenotypeE Vilain, B Le Fiblec, N Morichon-Delvallez, et al.
Journal of Medical Genetics|January 5, 2002
Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophyJ Amiel, V Raclin, J M Jouannic, et al.
Prenatal Diagnosis|April 1, 1989
Chromosomal prenatal diagnosis: study of 936 cases of intrauterine abnormalities after ultrasound assessmentP Eydoux, A Choiset, N Le Porrier, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics|July 7, 2000
Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow upD Sanlaville, M C Aubry, Y Dumez, et al.
Human Reproduction (Oxford, England)|February 3, 2007
Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case reportValérie Malan, R Gesny, N Morichon-Delvallez, et al.
Prenatal Diagnosis|June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann featuresS Fert-Ferrer, A Guichet, J Tantau, et al.
Human Mutation|September 23, 1998
Identification of novel L1CAM mutations using fluorescence-assisted mismatch analysisP Saugier-Veber, C Martin, N Le Meur, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Lancet (London, England)|January 22, 1994
SRY-negative XX fetus with complete male phenotypeE Vilain, B Le Fiblec, N Morichon-Delvallez, et al.
Journal of Medical Genetics|January 5, 2002
Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophyJ Amiel, V Raclin, J M Jouannic, et al.
Prenatal Diagnosis|April 1, 1989
Chromosomal prenatal diagnosis: study of 936 cases of intrauterine abnormalities after ultrasound assessmentP Eydoux, A Choiset, N Le Porrier, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.
Journal of Medical Genetics|July 7, 2000
Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow upD Sanlaville, M C Aubry, Y Dumez, et al.
Human Reproduction (Oxford, England)|February 3, 2007
Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case reportValérie Malan, R Gesny, N Morichon-Delvallez, et al.
Prenatal Diagnosis|June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann featuresS Fert-Ferrer, A Guichet, J Tantau, et al.
Human Mutation|September 23, 1998
Identification of novel L1CAM mutations using fluorescence-assisted mismatch analysisP Saugier-Veber, C Martin, N Le Meur, et al.
Pageof 4