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Author/Creator Le Vaillant, Claudine

2. Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases. (3rd November 2015)

Authors:
Allaf, Bichr; Dreux, Sophie; Schmitz, Thomas; Czerkiewicz, Isabelle; Le Vaillant, Claudine; Benachi, Alexandra; Houfflin‐Debarge, Véronique; Maréchaud, Martine; Oury, Jean‐François; Muller, Françoise
Journal:
Prenatal diagnosis
Issue:
Volume 35:Number 13(2015:Dec.)
Page Start:
1331
Record Type:
Journal Article
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3. Blepharophimosis, short humeri, developmental delay and hirschsprung disease: Expanding the phenotypic spectrum of MED12 mutations. Issue 7 (8th April 2014)

Authors:
Isidor, Bertrand; Lefebvre, Tiphaine; Le Vaillant, Claudine; Caillaud, Gaëlle; Faivre, Laurence; Jossic, Frédéric; Joubert, Madeleine; Winer, Norbert; Le Caignec, Cédric; Borck, Guntram; Pelet, Anna; Amiel, Jeanne; Toutain, Annick; Ronce, Nathalie; Raynaud, Martine; Verloes, Alain; David, Albert
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 7(2014.)
Page Start:
1821
Record Type:
Journal Article
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4. Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis. Issue 5 (12th December 2022)

Authors:
Ghesh, Leïla; Désir, Julie; Haye, Damien; Le Tanno, Pauline; Devillard, Françoise; Cogné, Benjamin; Marangoni, Martina; Tecco, Laura; Heron, Delphine; Le Vaillant, Claudine; Joubert, Madeleine; Beneteau, Claire
Journal:
Clinical genetics
Issue:
Volume 103:Issue 5(2023)
Page Start:
560
Record Type:
Journal Article
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5. Perinatal prognosis of pregnancies complicated by placental chronic villitis or intervillositis of unknown etiology and combined lesions: About a series of 178 cases. (August 2016)

Authors:
Nowak, Christel; Joubert, Madeleine; Jossic, Frederique; Masseau, Agathe; Hamidou, Mohamed; Philippe, Henri-Jean; Le Vaillant, Claudine
Journal:
Placenta
Issue:
Volume 44(2016:Aug.)
Page Start:
104
Record Type:
Journal Article
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7. Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series. (11th December 2021)

Authors:
Lesieur‐Sebellin, Marion; Till, Marianne; Khau Van Kien, Philippe; Herve, Bérénice; Bourgon, Nicolas; Dupont, Céline; Tabet, Anne‐Claude; Barrois, Mathilde; Coussement, Aurélie; Loeuillet, Laurence; Mousty, Eve; Ea, Vuthy; El Assal, Amal; Mary, Laura; Jaillard, Sylvie; Beneteau, Claire; Le Vailla...
Journal:
Prenatal diagnosis
Issue:
Volume 42:Number 1(2022)
Page Start:
118
Record Type:
Journal Article
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8. The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome. Issue 4 (13th July 2021)

Authors:
Ghesh, Leïla; Musquer, Marie Denis; Devisme, Louise; Stichelbout, Morgane; Boutaud, Lucile; Elkhartoufi, Nadia; Vaast, Pascal; Boute, Odile; Riteau, Anne‐Sophie; Le Vaillant, Claudine; Winer, Norbert; Joubert, Madeleine; Bezieau, Stéphane; Thomas, Sophie; Attie‐Bitach, Tania; Beneteau, Claire
Journal:
Clinical genetics
Issue:
Volume 100:Issue 4(2021)
Page Start:
462
Record Type:
Journal Article
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