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

Year Number of Results
1974 2
1976 1
1977 1
1978 2
1981 3
1982 2
1983 1
1984 1
1986 2
1987 2
1988 1
1990 1
1991 1
1992 1
1994 2
1995 3
1996 5
1997 2
1998 1
1999 5
2000 2
2001 1
2002 2
2003 4
2004 2
2005 4
2006 3
2007 7
2008 3
2009 4
2010 7
2011 1
2012 4
2013 5
2014 1
2015 1
2016 1
2017 3
2018 7
2019 3
2020 3
2021 4
2022 5
2023 1
2024 2

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110 results

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Page 1
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Caldas Rosa ECC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban-Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Lima AR, et al. Among authors: vianna morgante am. Hum Mutat. 2022 Jul;43(7):900-918. doi: 10.1002/humu.24375. Epub 2022 May 10. Hum Mutat. 2022. PMID: 35344616 Free PMC article.
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes.
Costa CIS, da Silva Montenegro EM, Zarrei M, de Sá Moreira E, Silva IMW, de Oliveira Scliar M, Wang JYT, Zachi EC, Branco EV, da Costa SS, Lourenço NCV, Vianna-Morgante AM, Rosenberg C, Krepischi ACV, Scherer SW, Passos-Bueno MR. Costa CIS, et al. Among authors: vianna morgante am. Clin Genet. 2022 Jan;101(1):134-141. doi: 10.1111/cge.14072. Epub 2021 Nov 15. Clin Genet. 2022. PMID: 34664255
Skewed X-chromosome Inactivation in Women with Idiopathic Intellectual Disability is Indicative of Pathogenic Variants.
Chaves LD, Carvalho LML, Tolezano GC, Pires SF, Costa SS, de Scliar MO, Giuliani LR, Bertola DR, Santos-Rebouças CB, Seo GH, Otto PA, Rosenberg C, Vianna-Morgante AM, Krepischi ACV. Chaves LD, et al. Among authors: vianna morgante am. Mol Neurobiol. 2023 Jul;60(7):3758-3769. doi: 10.1007/s12035-023-03311-0. Epub 2023 Mar 21. Mol Neurobiol. 2023. PMID: 36943625
The fragile x-associated tremor and ataxia syndrome (FXTAS).
Capelli LP, Gonçalves MR, Leite CC, Barbosa ER, Nitrini R, Vianna-Morgante AM. Capelli LP, et al. Among authors: vianna morgante am. Arq Neuropsiquiatr. 2010 Oct;68(5):791-8. doi: 10.1590/s0004-282x2010000500023. Arq Neuropsiquiatr. 2010. PMID: 21049196 Free article. Review.
Encomium: Oswaldo Frota-Pessoa.
Vianna-Morgante AM, Azevêdo ES, Otto PA, Opitz JM. Vianna-Morgante AM, et al. Am J Med Genet. 1996 Jun 28;63(4):581-4. doi: 10.1002/(SICI)1096-8628(19960628)63:4<581::AID-AJMG12>3.0.CO;2-E. Am J Med Genet. 1996. PMID: 8826438 No abstract available.
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses.
Villela D, Mazzonetto PC, Migliavacca MP, Perrone E, Guida G, Milanezi MFG, Jorge AAL, Ribeiro-Bicudo LA, Kok F, Campagnari F, de Rosso-Giuliani L, da Costa SS, Vianna-Morgante AM, Pearson PL, Krepischi ACV, Rosenberg C. Villela D, et al. Among authors: vianna morgante am. Am J Med Genet A. 2021 Aug;185(8):2335-2344. doi: 10.1002/ajmg.a.62237. Epub 2021 May 14. Am J Med Genet A. 2021. PMID: 33988290
Chromosome imbalances in syndromic hearing loss.
Catelani AL, Krepischi AC, Kim CA, Kok F, Otto PA, Auricchio MT, Mazzeu JF, Uehara DT, Costa SS, Knijnenburg J, Tabith A Jr, Vianna-Morgante AM, Mingroni-Netto RC, Rosenberg C. Catelani AL, et al. Among authors: vianna morgante am. Clin Genet. 2009 Nov;76(5):458-64. doi: 10.1111/j.1399-0004.2009.01276.x. Epub 2009 Oct 6. Clin Genet. 2009. PMID: 19807740
Phenotypic spectrum of 45,X/46,XY individuals.
Rosenberg C, Frota-Pessoa O, Vianna-Morgante AM, Chu TH. Rosenberg C, et al. Among authors: vianna morgante am. Am J Med Genet. 1987 Jul;27(3):553-9. doi: 10.1002/ajmg.1320270308. Am J Med Genet. 1987. PMID: 3631129
110 results