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M Valduga

Showing results (1-10 of 7) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 3, 2017
[22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis]T Ingrao, L Lambert, M Valduga, et al.
European Journal of Medical Genetics|September 1, 2007
Prenatal diagnosis of mosaicism for 11q terminal deletionM Valduga, V Latger Cannard, C Philippe, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri-du-chat syndromeA L Mosca, P Callier, B Leheup, et al.
Prenatal Diagnosis|February 16, 2010
A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformationsM Valduga, C Philippe, P Bach Segura, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 14, 2017
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter studyM Egloff, B Hervé, T Quibel, et al.
Prenatal Diagnosis|June 26, 2014
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 casesN Gruchy, F Vialard, E Blondeel, et al.
Prenatal Diagnosis|January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesJ Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 3, 2017
[22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis]T Ingrao, L Lambert, M Valduga, et al.
European Journal of Medical Genetics|September 1, 2007
Prenatal diagnosis of mosaicism for 11q terminal deletionM Valduga, V Latger Cannard, C Philippe, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri-du-chat syndromeA L Mosca, P Callier, B Leheup, et al.
Prenatal Diagnosis|February 16, 2010
A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformationsM Valduga, C Philippe, P Bach Segura, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 14, 2017
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter studyM Egloff, B Hervé, T Quibel, et al.
Prenatal Diagnosis|June 26, 2014
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 casesN Gruchy, F Vialard, E Blondeel, et al.
Prenatal Diagnosis|January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesJ Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Pageof 1