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Page 1
Craniofacial growth and function in achondroplasia: a multimodal 3D study on 15 patients.
Morice A, Taverne M, Eché S, Griffon L, Fauroux B, Leboulanger N, Couloigner V, Baujat G, Cormier-Daire V, Picard A, Legeai-Mallet L, Kadlub N, Khonsari RH. Morice A, et al. Among authors: picard a. Orphanet J Rare Dis. 2023 Apr 18;18(1):88. doi: 10.1186/s13023-023-02664-y. Orphanet J Rare Dis. 2023. PMID: 37072824 Free PMC article.
Normative data on nasalance scores for French speaking children.
Barbier H, Redouloux L, Chapuis-Vandenbogaerde C, Picard A, Amelot A, Fougeron C, Sanquer E, Kadlub N. Barbier H, et al. Among authors: picard a. J Stomatol Oral Maxillofac Surg. 2024 Sep 21;126(3):102089. doi: 10.1016/j.jormas.2024.102089. Online ahead of print. J Stomatol Oral Maxillofac Surg. 2024. PMID: 39313155
Next generation phenotyping for diagnosis and phenotype-genotype correlations in Kabuki syndrome.
Hennocq Q, Willems M, Amiel J, Arpin S, Attie-Bitach T, Bongibault T, Bouygues T, Cormier-Daire V, Corre P, Dieterich K, Douillet M, Feydy J, Galliani E, Giuliano F, Lyonnet S, Picard A, Porntaveetus T, Rio M, Rouxel F, Shotelersuk V, Toutain A, Yauy K, Geneviève D, Khonsari RH, Garcelon N. Hennocq Q, et al. Among authors: picard a. Sci Rep. 2024 Jan 28;14(1):2330. doi: 10.1038/s41598-024-52691-3. Sci Rep. 2024. PMID: 38282012 Free PMC article.
An automatic facial landmarking for children with rare diseases.
Hennocq Q, Bongibault T, Bizière M, Delassus O, Douillet M, Cormier-Daire V, Amiel J, Lyonnet S, Marlin S, Rio M, Picard A, Khonsari RH, Garcelon N. Hennocq Q, et al. Among authors: picard a. Am J Med Genet A. 2023 May;191(5):1210-1221. doi: 10.1002/ajmg.a.63126. Epub 2023 Jan 30. Am J Med Genet A. 2023. PMID: 36714960
Biallelic truncating variants in VGLL2 cause syngnathia in humans.
Agostini V, Tessier A, Djaziri N, Khonsari RH, Galliani E, Kurihara Y, Honda M, Kurihara H, Hidaka K, Tuncbilek G, Picard A, Konas E, Amiel J, Gordon CT. Agostini V, et al. Among authors: picard a. J Med Genet. 2023 Nov;60(11):1084-1091. doi: 10.1136/jmg-2022-109059. Epub 2023 Sep 4. J Med Genet. 2023. PMID: 37666660
440 results