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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1986 1
1987 1
1988 5
1989 3
1990 2
1995 2
1996 2
1998 2
1999 4
2000 2
2001 3
2003 1
2004 3
2006 5
2007 4
2008 3
2009 6
2010 4
2011 7
2012 6
2013 4
2014 8
2015 6
2016 5
2017 4
2018 3
2019 11
2020 9
2021 5
2022 4
2023 1
2024 0

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103 results

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Page 1
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.
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
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
[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.
The GAPO syndrome.
Manouvrier-Hanu S, Largilliere C, Benalioua M, Farriaux JP, Fontaine G. Manouvrier-Hanu S, et al. Am J Med Genet. 1987 Mar;26(3):683-8. doi: 10.1002/ajmg.1320260323. Am J Med Genet. 1987. PMID: 3565482
TRIT1 deficiency: Two novel patients with four novel variants.
Smol T, Brunelle P, Caumes R, Boute-Benejean O, Thuillier C, Figeac M, Ait-Yahya E, Bonte F, Mau-Them FT, Thauvin-Robinet C, Faivre L, Roche-Lestienne C, Manouvrier-Hanu S, Petit F, Ghoumid J. Smol T, et al. Among authors: manouvrier hanu s. Eur J Med Genet. 2022 Nov;65(11):104603. doi: 10.1016/j.ejmg.2022.104603. Epub 2022 Aug 29. Eur J Med Genet. 2022. PMID: 36049610
103 results