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N Morichon

Showing results (11-20 of 31) with videos related to

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Prenatal Diagnosis|November 1, 1993
Serum hCG assay: a method for detection of contamination of fetal blood samplesM Dommergues, V Bunduki, F Muller, et al.
Journal De Genetique Humaine|September 1, 1983
[Solitary upper incisor, hypopituitarism and monosomy 18p chromosome aberration]B Boudailliez, N Morichon-Delvallez, A Goldfarb, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Contribution of genetics]S Lyonnet, N Morichon, M Dommergues, et al.
Fetal Diagnosis and Therapy|May 1, 1996
First-trimester translucency: aneuploidy, sonographic findings, and maternal ageD Mahieu-Caputo, M Dommergues, N Morichon-Delvallez, et al.
Early Human Development|June 1, 1993
Anti-müllerian hormone in early human developmentN Josso, I Lamarre, J Y Picard, et al.
European Journal of Medical Genetics|December 5, 2006
Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletionM Chaabouni, J Martinovic, D Sanlaville, et al.
American Journal of Medical Genetics|March 17, 1997
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeV Cormier-Daire, M Le Merrer, N Gigarel, et al.
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.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|November 1, 1993
Serum hCG assay: a method for detection of contamination of fetal blood samplesM Dommergues, V Bunduki, F Muller, et al.
Journal De Genetique Humaine|September 1, 1983
[Solitary upper incisor, hypopituitarism and monosomy 18p chromosome aberration]B Boudailliez, N Morichon-Delvallez, A Goldfarb, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Contribution of genetics]S Lyonnet, N Morichon, M Dommergues, et al.
Fetal Diagnosis and Therapy|May 1, 1996
First-trimester translucency: aneuploidy, sonographic findings, and maternal ageD Mahieu-Caputo, M Dommergues, N Morichon-Delvallez, et al.
Early Human Development|June 1, 1993
Anti-müllerian hormone in early human developmentN Josso, I Lamarre, J Y Picard, et al.
European Journal of Medical Genetics|December 5, 2006
Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletionM Chaabouni, J Martinovic, D Sanlaville, et al.
American Journal of Medical Genetics|March 17, 1997
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeV Cormier-Daire, M Le Merrer, N Gigarel, et al.
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.
Pageof 4