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V Malan

Showing results (1-10 of 25) 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|April 3, 2019
ReplyM Egloff, V Malan
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 21, 2012
[Diagnosis of chromosomal abnormalities by array CGH in constitutional pathology: the end of the first-line karyotype]V Malan, S Romana
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|November 12, 2013
[Managing and identifying the causes of IUGR]L J Salomon, V Malan
Clinical Genetics|October 10, 2006
Chimera and other fertilization errorsV Malan, M Vekemans, C Turleau
Gynecologie, Obstetrique & Fertilite|November 15, 2016
[Cell-free fetal DNA screening tests for trisomy 21]V Malan, L Bussières, L J Salomon
The Journal of Urology|January 16, 2007
The long-term followup of 33 cases of true hermaphroditism: a 40-year experience with conservative gonadal surgeryG Verkauskas, F Jaubert, S Lortat-Jacob, et al.
Prenatal Diagnosis|February 5, 2008
First prenatally diagnosed case of 16p11.2p12.1 duplicationS Bourthoumieu, F Esclaire, F Terro, et al.
Clinical Genetics|July 14, 2011
Maternal uniparental disomy of chromosome 16 in a patient with adenine phosphoribosyltransferase deficiencyI Ceballos-Picot, G Guest, V Moriniere, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 23, 2019
Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysisA Le Bras, L J Salomon, L Bussières, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
A new case of a severe clinical phenotype of the cat-eye syndromeT Martin Denavit, V Malan, C Grillon, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 3, 2019
ReplyM Egloff, V Malan
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 21, 2012
[Diagnosis of chromosomal abnormalities by array CGH in constitutional pathology: the end of the first-line karyotype]V Malan, S Romana
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|November 12, 2013
[Managing and identifying the causes of IUGR]L J Salomon, V Malan
Clinical Genetics|October 10, 2006
Chimera and other fertilization errorsV Malan, M Vekemans, C Turleau
Gynecologie, Obstetrique & Fertilite|November 15, 2016
[Cell-free fetal DNA screening tests for trisomy 21]V Malan, L Bussières, L J Salomon
The Journal of Urology|January 16, 2007
The long-term followup of 33 cases of true hermaphroditism: a 40-year experience with conservative gonadal surgeryG Verkauskas, F Jaubert, S Lortat-Jacob, et al.
Prenatal Diagnosis|February 5, 2008
First prenatally diagnosed case of 16p11.2p12.1 duplicationS Bourthoumieu, F Esclaire, F Terro, et al.
Clinical Genetics|July 14, 2011
Maternal uniparental disomy of chromosome 16 in a patient with adenine phosphoribosyltransferase deficiencyI Ceballos-Picot, G Guest, V Moriniere, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 23, 2019
Cost-effectiveness of five prenatal screening strategies for trisomies and other unbalanced chromosomal abnormalities: model-based analysisA Le Bras, L J Salomon, L Bussières, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
A new case of a severe clinical phenotype of the cat-eye syndromeT Martin Denavit, V Malan, C Grillon, et al.
Pageof 3