Ferrari I - Search Results

1

Concurrent Loss of Heterozygosity and Mosaic Deletion of 12p13.32pter.

Faria RS, de Oliveira CP, da Costa MM, da S Rosa MT, Córdoba MS, Pic-Taylor A, Ferrari I, de Oliveira SF, Mazzeu JF. Faria RS, et al. Among authors: ferrari i. Cytogenet Genome Res. 2016;148(2-3):174-8. doi: 10.1159/000445853. Epub 2016 Jun 2. Cytogenet Genome Res. 2016. PMID: 27251740

2

Transient neonatal hypothyroidism in a boy with unbalanced translocation t(8;16).

Secchi LA, Mazzeu JF, Córdoba MS, Ferrari I, Ramos HE, Neves Fde A. Secchi LA, et al. Among authors: ferrari i. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):564-9. doi: 10.1590/s0004-27302012000800017. Arq Bras Endocrinol Metabol. 2012. PMID: 23295299

3

Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum.

Dos Santos PA, de Oliveira SF, Freitas EL, Safatle HP, Rosenberg C, Ferrari I, Mazzeu JF. Dos Santos PA, et al. Among authors: ferrari i. Am J Med Genet A. 2014 Feb;164A(2):551-3. doi: 10.1002/ajmg.a.36231. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311469 No abstract available.

4

Partial AFF2 microduplication in a patient with auditory processing disorder, emotional impairment and macrosomia.

da Rocha NB, dos Santos PA, Safatle HP, de Melo RM, Pereira RW, de Oliveira SF, Pic-Taylor A, Ferrari I, Mazzeu JF. da Rocha NB, et al. Among authors: ferrari i. Am J Med Genet A. 2014 Dec;164A(12):3206-8. doi: 10.1002/ajmg.a.36768. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25256661 No abstract available.

5

Partial 1q Duplications and Associated Phenotype.

Morris ML, Baroneza JE, Teixeira P, Medina CT, Cordoba MS, Versiani BR, Roese LL, Freitas EL, Fonseca AC, Dos Santos MC, Pic-Taylor A, Rosenberg C, Oliveira SF, Ferrari I, Mazzeu JF. Morris ML, et al. Among authors: ferrari i. Mol Syndromol. 2016 Feb;6(6):297-303. doi: 10.1159/000443599. Epub 2016 Feb 4. Mol Syndromol. 2016. PMID: 27022331 Free PMC article.

6

Complex phenotype associated with 17q21.31 microdeletion.

Dornelles-Wawruk H, Pic-Taylor A, Rosenberg C, Krepischi AC, Safatle HP, Ferrari I, Mazzeu JF. Dornelles-Wawruk H, et al. Among authors: ferrari i. Mol Syndromol. 2013 Sep;4(6):297-301. doi: 10.1159/000354120. Epub 2013 Aug 21. Mol Syndromol. 2013. PMID: 24167466 Free PMC article.

7

Analysis of GATA1 mutations and leukemogenesis in newborns with Down syndrome.

Queiroz LB, Lima BD, Mazzeu JF, Camargo R, Córdoba MS, Q Magalhães I, Martins-de-Sá C, Ferrari I. Queiroz LB, et al. Among authors: ferrari i. Genet Mol Res. 2013 Oct 18;12(4):4630-8. doi: 10.4238/2013.October.18.1. Genet Mol Res. 2013. PMID: 24222239 Free article.

8

Molecular and chromosomal mutations among children with B-lineage lymphoblastic leukemia in Brazil's Federal District.

Mesquita DR, Córdoba JC, Magalhães IQ, Córdoba MS, Oliveira JR, Gonçalves A, Ferrari I, Martins-de-Sá C. Mesquita DR, et al. Among authors: ferrari i. Genet Mol Res. 2009 Mar 24;8(1):345-53. doi: 10.4238/vol8-1gmr582. Genet Mol Res. 2009. PMID: 19440970 Free article.

9

Transient neonatal myeloproliferative disorder without Down syndrome and detection of GATA1 mutation.

Magalhães IQ, Splendore A, Emerenciano M, Córdoba MS, Córdoba JC, Allemand PA, Ferrari I, Pombo-de-Oliveira MS. Magalhães IQ, et al. Among authors: ferrari i. J Pediatr Hematol Oncol. 2005 Jan;27(1):50-2. doi: 10.1097/01.mph.0000151801.26478.03. J Pediatr Hematol Oncol. 2005. PMID: 15654280

10

Craniofacial and dental features in kabuki syndrome patients.

do Prado Sobral S, Leite AF, Figueiredo PT, Ferrari I, Safatle HP, Córdoba MS, Versiani BR, Acevedo AC, Mestrinho HD. do Prado Sobral S, et al. Among authors: ferrari i. Cleft Palate Craniofac J. 2013 Jul;50(4):440-7. doi: 10.1597/11-052. Epub 2011 Oct 24. Cleft Palate Craniofac J. 2013. PMID: 22023252

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