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N Morichon-Delvallez

Showing results (11-20 of 20) with videos related to

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Prenatal Diagnosis|December 2, 2009
Gestational age-related reference values for amniotic fluid organic acidsC Ottolenghi, N Abermil, A Lescoat, et al.
Prenatal Diagnosis|September 24, 2004
Prenatal diagnosis and characterization of an analphoid marker chromosome 16A C Tabet, P Gosset, H Elghezal, et al.
American Journal of Medical Genetics|March 21, 1998
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7qG H Vance, C Nickerson, L Sarnat, 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.
Journal of Medical Genetics|September 20, 2005
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human developmentD Sanlaville, H C Etchevers, M Gonzales, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Prenatal Diagnosis|December 2, 2009
Gestational age-related reference values for amniotic fluid organic acidsC Ottolenghi, N Abermil, A Lescoat, et al.
Prenatal Diagnosis|September 24, 2004
Prenatal diagnosis and characterization of an analphoid marker chromosome 16A C Tabet, P Gosset, H Elghezal, et al.
American Journal of Medical Genetics|March 21, 1998
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7qG H Vance, C Nickerson, L Sarnat, 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.
Journal of Medical Genetics|September 20, 2005
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human developmentD Sanlaville, H C Etchevers, M Gonzales, et al.
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