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

Year Number of Results
1981 1
1983 2
1985 1
1986 1
1987 3
1988 1
1990 2
1991 2
1992 3
1993 3
1995 2
1996 4
1997 2
1998 3
1999 2
2004 3
2005 3
2006 2
2007 7
2008 9
2009 7
2010 7
2011 10
2012 4
2013 10
2014 2
2015 7
2016 6
2017 7
2018 6
2019 2
2020 2
2021 4
2022 3
2023 1
2024 0

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121 results

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Page 1
[Odontochondrodysplasia].
Maroteaux P, Briscioli V, Lalatta F, Bonaventure J. Maroteaux P, et al. Among authors: lalatta f. Arch Pediatr. 1996 Jun;3(6):549-54. doi: 10.1016/0929-693x(96)83225-8. Arch Pediatr. 1996. PMID: 8881299 French.
Prenatal diagnosis of Simpson-Golabi-Behmel syndrome.
Magini P, Palombo F, Boito S, Lanzoni G, Mongelli P, Rizzuti T, Baccarin M, Pippucci T, Seri M, Lalatta F. Magini P, et al. Among authors: lalatta f. Am J Med Genet A. 2016 Dec;170(12):3258-3264. doi: 10.1002/ajmg.a.37873. Epub 2016 Sep 9. Am J Med Genet A. 2016. PMID: 27612164
Retinoblastoma, chromosome abnormalities and oncogene expression.
Gilbert F, Potluri VR, Short MP, Kau CL, Lalatta F. Gilbert F, et al. Among authors: lalatta f. Ophthalmic Paediatr Genet. 1987 Mar;8(1):3-10. doi: 10.3109/13816818709028508. Ophthalmic Paediatr Genet. 1987. PMID: 3295640 Review.
Family burden of children suffering from epidermolysis bullosa.
DE Stefano S, Grassi FS, Lalatta F, Scuvera G, Brena M, Grillo P, Peves Rios WE, Guez S. DE Stefano S, et al. Among authors: lalatta f. Ital J Dermatol Venerol. 2021 Oct;156(5):580-587. doi: 10.23736/S2784-8671.20.06613-4. Epub 2020 Oct 9. Ital J Dermatol Venerol. 2021. PMID: 33034432
Maternal input to children with sex chromosome trisomies.
Zampini L, Ferrante C, Silibello G, Dall'Ara F, Rigamonti C, Zanchi P, Vizziello PG, Lalatta F, Costantino MA. Zampini L, et al. Among authors: lalatta f. Int J Lang Commun Disord. 2020 Sep;55(5):724-733. doi: 10.1111/1460-6984.12557. Epub 2020 Jul 7. Int J Lang Commun Disord. 2020. PMID: 32634287
121 results