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Showing results for manouvrier hanu s
Search for Manouvier-Hanu S instead (1 results)
Phenotypic spectrum of SHANK2-related neurodevelopmental disorder.
Caumes R, Smol T, Thuillier C, Balerdi M, Lestienne-Roche C, Manouvrier-Hanu S, Ghoumid J. Caumes R, et al. Among authors: manouvrier hanu s. Eur J Med Genet. 2020 Dec;63(12):104072. doi: 10.1016/j.ejmg.2020.104072. Epub 2020 Sep 25. Eur J Med Genet. 2020. PMID: 32987185 Review.
[Twins].
Manouvrier-Hanu S. Manouvrier-Hanu S. LARC Med. 1983 Oct;3(8):561-70. LARC Med. 1983. PMID: 6664194 French. No abstract available.
Genetics of limb anomalies in humans.
Manouvrier-Hanu S, Holder-Espinasse M, Lyonnet S. Manouvrier-Hanu S, et al. Trends Genet. 1999 Oct;15(10):409-17. doi: 10.1016/s0168-9525(99)01823-5. Trends Genet. 1999. PMID: 10498937 Review.
Neurodevelopmental phenotype associated with CHD8-SUPT16H duplication.
Smol T, Thuillier C, Boudry-Labis E, Dieux-Coeslier A, Duban-Bedu B, Caumes R, Bouquillon S, Manouvrier-Hanu S, Roche-Lestienne C, Ghoumid J. Smol T, et al. Among authors: manouvrier hanu s. Neurogenetics. 2020 Jan;21(1):67-72. doi: 10.1007/s10048-019-00599-w. Epub 2019 Dec 10. Neurogenetics. 2020. PMID: 31823155
Aarskog-Scott syndrome: a clinical study based on a large series of 111 male patients with a pathogenic variant in FGD1 and management recommendations.
Jeanne M, Ronce N, Remizé S, Arpin S, Baujat G, Breton S, Petit F, Vanlerberghe C, Coeslier-Dieux A, Manouvrier-Hanu S, Vincent-Delorme C, Khau Van Kien P, Van-Gils J, Quélin C, Pasquier L, Odent S, Demurger F, Laffargue F, Francannet C, Martin-Coignard D, Afenjar A, Whalen S, Verloes A, Capri Y, Delahaye A, Plaisancié J, Labrune P, Destree A, Maystadt I, Ciorna Monferrato V, Isidor B, Vincent M, Jean Marçais N, Nambot S, Schaefer E, El Chehadeh S, Lespinasse J, Collignon P, Busa T, Philip N, Willems M, Planes M, Vanakker OM, Lambert L, Leheup B, Mathieu-Dramard M, Morin G, Dieterich K, Ginglinger E, Bayat A, Balasubramanian M, Dauriat B, Haye D, Amiel J, Rio M, Cormier-Daire V, Toutain A. Jeanne M, et al. Among authors: manouvrier hanu s. J Med Genet. 2025 Mar 20;62(4):258-267. doi: 10.1136/jmg-2022-108868. J Med Genet. 2025. PMID: 39798962 Free article.
Townes-Brocks syndrome: genotype-phenotype correlations of SALL1 variants in our series and the literature.
Leduc F, Brunelle P, Escande F, Ramdane N, Bellengier L, Giacomello L, Lefevre C, Mezel A, Samaille C, Sfeir R, Toulemonde P; Rare Disease networks; Manouvrier-Hanu S, Vincent-Delorme C, Petit F, Vanlerberghe C. Leduc F, et al. Among authors: manouvrier hanu s. Eur J Hum Genet. 2025 May 10. doi: 10.1038/s41431-025-01855-4. Online ahead of print. Eur J Hum Genet. 2025. PMID: 40348827
Fraser syndrome without cryptophthalmos: Two cases.
Boussion S, Lyonnet S, Van Der Zwaag B, Vogel MJ, Smol T, Mezel A, Manouvrier-Hanu S, Vincent-Delorme C, Vanlerberghe C. Boussion S, et al. Among authors: manouvrier hanu s. Eur J Med Genet. 2020 Apr;63(4):103839. doi: 10.1016/j.ejmg.2020.103839. Epub 2020 Jan 7. Eur J Med Genet. 2020. PMID: 31923588
Executive functioning in adolescents and adults with Silver-Russell syndrome.
Burgevin M, Lacroix A, Ollivier F, Bourdet K, Coutant R, Donadille B, Faivre L, Manouvrier-Hanu S, Petit F, Thauvin-Robinet C, Toutain A, Netchine I, Odent S. Burgevin M, et al. Among authors: manouvrier hanu s. PLoS One. 2023 Jan 20;18(1):e0279745. doi: 10.1371/journal.pone.0279745. eCollection 2023. PLoS One. 2023. PMID: 36662731 Free PMC article.
106 results