Search research articles
Contact Us
Filters
Showing results (11-20 of 16) with videos related to
Page
of 2
Sort By:
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 study
M Nkobetchou, M Leruez-Ville, T Guilleminot, et al.
Clinical Genetics
|
March 7, 2018
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder
J 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 obstruction
E 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 syndrome
C Dupont, F Guimiot, L Perrin, et al.
Neurology
|
September 23, 2009
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations
S Passemard, L Titomanlio, M Elmaleh, et al.
Human Mutation
|
June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephaly
C Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 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 study
M Nkobetchou, M Leruez-Ville, T Guilleminot, et al.
Clinical Genetics
|
March 7, 2018
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder
J 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 obstruction
E 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 syndrome
C Dupont, F Guimiot, L Perrin, et al.
Neurology
|
September 23, 2009
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations
S Passemard, L Titomanlio, M Elmaleh, et al.
Human Mutation
|
June 15, 2007
Molecular heterogeneity in fetal forms of type II lissencephaly
C Bouchet, M Gonzales, S Vuillaumier-Barrot, et al.
Page
of 2