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

Year Number of Results
2006 1
2007 1
2008 3
2009 2
2010 6
2011 3
2012 8
2013 7
2014 10
2015 9
2016 3
2017 2
2018 4
2019 5
2020 12
2021 4
2022 10
2023 10
2024 4

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92 results

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Page 1
Cri-du-Chat Syndrome: Revealing a Familial Atypical Deletion in 5p.
Almeida VT, Chehimi SN, Gasparini Y, Nascimento AM, Carvalho GFS, Montenegro MM, Zanardo ÉA, Dias AT, Assunção NA, Kim CA, Kulikowski LD. Almeida VT, et al. Among authors: kulikowski ld. Mol Syndromol. 2023 Jan;13(6):527-536. doi: 10.1159/000524371. Epub 2022 May 18. Mol Syndromol. 2023. PMID: 36660031 Free PMC article.
The complex search for the cause of gastroschisis.
de Freitas AB, Francisco RPV, Hoshida MS, De Oliveira YG, Kulikowski LD, de Lourdes Brizot M. de Freitas AB, et al. Among authors: kulikowski ld. Birth Defects Res. 2022 Nov 15;114(19):1291-1297. doi: 10.1002/bdr2.2047. Epub 2022 May 16. Birth Defects Res. 2022. PMID: 35574732
Fetal gastroschisis: Maternal and fetal methylation profile.
Freitas AB, Francisco RPV, Centofanti SF, Damasceno JG, Chehimi SN, Osmundo-Junior GS, Kulikowski LD, Brizot ML. Freitas AB, et al. Among authors: kulikowski ld. Prenat Diagn. 2021 Mar;41(4):449-456. doi: 10.1002/pd.5881. Epub 2021 Jan 3. Prenat Diagn. 2021. PMID: 33332636
Ring chromosome 10: report on two patients and review of the literature.
Guilherme RS, Kim CA, Alonso LG, Honjo RS, Meloni VA, Christofolini DM, Kulikowski LD, Melaragno MI. Guilherme RS, et al. Among authors: kulikowski ld. J Appl Genet. 2013 Feb;54(1):35-41. doi: 10.1007/s13353-012-0128-7. Epub 2012 Dec 18. J Appl Genet. 2013. PMID: 23247912 Review.
Expanding the Phenotype of 8p23.1 Deletion Syndrome: Eight New Cases Resembling the Clinical Spectrum of 22q11.2 Microdeletion.
Montenegro MM, Camilotti D, Quaio CRDC, Gasparini Y, Zanardo ÉA, Rangel-Santos A, Novo-Filho GM, Francisco G, Liro L, Nascimento A, Chehimi SN, Soares DCQ, Krepischi ACV, Grassi MS, Honjo RS, Palmeira P, Kim CA, Carneiro-Sampaio MMS, Rosenberg C, Kulikowski LD. Montenegro MM, et al. Among authors: kulikowski ld. J Pediatr. 2023 Jan;252:56-60.e2. doi: 10.1016/j.jpeds.2022.08.051. Epub 2022 Sep 5. J Pediatr. 2023. PMID: 36067875
Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion.
Guilherme RS, Soares KC, Simioni M, Vieira TP, Gil-da-Silva-Lopes VL, Kim CA, Brunoni D, Spinner NB, Conlin LK, Christofolini DM, Kulikowski LD, Steiner CE, Melaragno MI. Guilherme RS, et al. Among authors: kulikowski ld. Am J Med Genet A. 2014 Jul;164A(7):1659-65. doi: 10.1002/ajmg.a.36512. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700634 Review.
92 results