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F Guimiot

Showing results (11-20 of 16) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 31, 2023
SARS-CoV-2 infection as cause of in-utero fetal death: regional multicenter cohort studyM Nkobetchou, M Leruez-Ville, T Guilleminot, et al.
Clinical Genetics|March 7, 2018
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorderJ Lévy, D Haye, N Marziliano, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 21, 2016
Sequential fetal serum β2-microglobulin to predict postnatal renal function in bilateral or low urinary tract obstructionE Spaggiari, G Faure, S Dreux, et al.
Clinical Genetics|May 11, 2011
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndromeC Dupont, F Guimiot, L Perrin, et al.
Neurology|September 23, 2009
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutationsS Passemard, L Titomanlio, M Elmaleh, et al.
Human Mutation|June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephalyC Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 31, 2023
SARS-CoV-2 infection as cause of in-utero fetal death: regional multicenter cohort studyM Nkobetchou, M Leruez-Ville, T Guilleminot, et al.
Clinical Genetics|March 7, 2018
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorderJ Lévy, D Haye, N Marziliano, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 21, 2016
Sequential fetal serum β2-microglobulin to predict postnatal renal function in bilateral or low urinary tract obstructionE Spaggiari, G Faure, S Dreux, et al.
Clinical Genetics|May 11, 2011
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndromeC Dupont, F Guimiot, L Perrin, et al.
Neurology|September 23, 2009
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutationsS Passemard, L Titomanlio, M Elmaleh, et al.
Human Mutation|June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephalyC Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Pageof 2