C. Le Vaillant

发表

Accuracy of Ultrasonography and Magnetic Resonance Imaging in the Diagnosis of Placenta Accreta

A. Benachi, S. Prévôt, M. Joubert, 2014, PloS one.

Prenatal Sonographic Patterns in Six Cases of Wolf-Hirschhorn (4p–) Syndrome

B. Benoit, A. Bongain, P. Parent, 2004, Fetal Diagnosis and Therapy.

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study

L. Salomon, C. Bénéteau, M. Vekemans, 2018, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome

N. Winer, C. Bénéteau, P. Vaast, 2021, Clinical genetics.

Blepharophimosis, short humeri, developmental delay and hirschsprung disease: Expanding the phenotypic spectrum of MED12 mutations

A. Toutain, N. Winer, A. Verloes, 2014, American journal of medical genetics. Part A.

Monozygotic triplet pregnancies after single blastocyst transfer: two cases and literature review.

P. Barrière, T. Fréour, L. Dessolle, 2010, Reproductive biomedicine online.

[Correlation between antenatal ultrasound and postnatal diagnosis in cleft lip or palate: A retrospective study of 44 cases].

P. Corre, V. Dochez, Anne-Sophie Riteau, 2015, Gynecologie, obstetrique & fertilite.

Prenatal sonographic findings in Peters‐plus syndrome

G. Boog, C. Le Vaillant, M. Joubert, 2005, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.

A. Raaijmakers, J. Oury, R. Favre, 2020, Kidney international.

Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series

P. Sonigo, L. Salomon, C. Bénéteau, 2021, Prenatal diagnosis.

Prenatal diagnosis of congenital dislocated spine and complex heterotaxy syndrome with 3D ultrasound and helical computed tomography

C. Bénéteau, A. Hamel, M. Joubert, 2020, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Perinatal prognosis of pregnancies complicated by placental chronic villitis or intervillositis of unknown etiology and combined lesions: About a series of 178 cases.

A. Masseau, M. Hamidou, M. Joubert, 2016, Placenta.

Termination of pregnancy following prenatal diagnosis of placenta percreta at 16 weeks.

C. Le Vaillant, X. Aireau, C. Frick, 2016, European journal of obstetrics, gynecology, and reproductive biology.

[When should evoke prenatal paternal uniparental disomy 14?].

C. Bénéteau, H. Philippe, C. Le Vaillant, 2014, Gynecologie, obstetrique & fertilite.

Prenatal Diagnosis of a ‘Minor’ Form of Brachmann-de Lange Syndrome by Three-Dimensional Sonography and Three-Dimensional Computed Tomography

A. David, G. Boog, M. Quéré, 2004, Fetal Diagnosis and Therapy.

Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops

C. Bénéteau, S. Blesson, C. Le Caignec, 2014, Clinical genetics.

A Gardos channelopathy associated with nonimmune hydrops and fetal loss

C. Bénéteau, T. Besnard, V. Picard, 2022, Clinical genetics.

[Is the bronchial atresia prenatal diagnosis possible?].

N. Winer, A. Paumier, G. Podevin, 2008, Gynecologie, obstetrique & fertilite.

[Combining corticosteroid and aspirin for the prevention of recurrent villitis or intervillositis of unknown etiology].

G. Boog, J. Muller, C. Le Vaillant, 2006, Journal de gynecologie, obstetrique et biologie de la reproduction.

Contribution of Tridimensional Sonography and Magnetic Resonance Imaging to Prenatal Diagnosis of Apert Syndrome at Mid-Trimester

N. Winer, A. David, G. Boog, 1999, Fetal Diagnosis and Therapy.

Prenatal diagnosis of enlarged prostatic utricle by ultrasonography and magnetic resonance imaging

Y. Heloury, G. Boog, G. Podevin, 2008, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases

J. Oury, A. Benachi, F. Muller, 2015, Prenatal diagnosis.

[Acardiac twins: pronostics markers' study].

N. Winer, G. Boog, H. Philippe, 2012, Gynecologie, obstetrique & fertilite.

[Monoamniotic twins: diagnosis and management].

N. Winer, H. Philippe, C. Le Vaillant, 2009, Journal de gynecologie, obstetrique et biologie de la reproduction.

Dehydrated hereditary stomatocytosis: Prenatal management of ascites and pleural effusions.

C. Bénéteau, Anne-Sophie Riteau, C. Le Vaillant, 2018, Taiwanese journal of obstetrics & gynecology.

A Pilot Study Comparing 2- and 3-dimensional Ultrasound Imaging for Confirmation of Essure Fallopian Tube Pregnancy Prevention Implants.

P. Lopes, C. Le Vaillant, Marine Godfroy, 2018, Journal of minimally invasive gynecology.

Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography

M. Vincent, M. Joubert, C. Le Vaillant, 2018, Journal of ultrasound in medicine.

Contribution of Three-Dimensional Ultrasonography in Depicting Perineal Features in Cloacal Malformation

H. Philippe, C. Le Vaillant, H. Le Borgne, 2011, Fetal Diagnosis and Therapy.

[Monoamniotic twins: diagnosis and management].

N. Winer, N. Winer, H. Philippe, 2009, Journal de gynecologie, obstetrique et biologie de la reproduction.

Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis

C. Bénéteau, B. Cogné, D. Heron, 2022, Clinical genetics.

Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities.

A. Kaykas, C. Bénéteau, B. Cogné, 2023, Genetics in medicine : official journal of the American College of Medical Genetics.