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Oral phenotype in SATB2-associated syndrome: cross-sectional study of the French cohort

Title:	Oral phenotype in SATB2-associated syndrome: cross-sectional study of the French cohort
Authors:	Vegas, Nancy^{Aff1, Aff2, Aff3, Aff4, IDs13023025036093_cor1}; Rio, Marlène^Aff5; Adnot, Pauline^{Aff1, Aff3, Aff4}; Soupre, Véronique^{Aff4, Aff6}; Petit, Florence^Aff7; Ghoumid, Jamal^Aff7; Toutain, Annick^Aff8; Dieterich, Klaus^Aff9; Marey, Isabelle^Aff9; Gilbert-Dussardier, Brigitte^Aff10; Le Guyader, Gwenaël^Aff10; Francannet, Christine^Aff11; Schaefer, Elise^Aff12; Perrin, Laurence^Aff13; Nizon, Mathilde^Aff14; Beneteau, Claire^Aff14; Genevieve, David^Aff15; Willems, Marjolaine^Aff15; Faivre, Laurence^Aff16; Grimaldi, Marianne^Aff16; Melki, Judith^Aff17; Stoeva, Radka^Aff18; Putoux, Audrey^Aff19; Pons, Linda^Aff20; Benistan, Karelle^Aff21; Amiel, Jeanne^{Aff2, Aff3, Aff5}; Abadie, Véronique^{Aff1, Aff3, Aff4}
Source:	Orphanet Journal of Rare Diseases. 20(1)
Database:	Springer Nature Journals