Cavalcanti DP - Search Results

1

Two cases of Y; autosome translocations: A 45,X male and a clinically trisomy 18 patient.

Farah SB, Ramos CF, de Mello MP, Sartorato EL, Horelli-Kuitunen N, Lopes VL, Cavalcanti DP, Hackel C. Farah SB, et al. Among authors: cavalcanti dp. Am J Med Genet. 1994 Feb 15;49(4):388-92. doi: 10.1002/ajmg.1320490407. Am J Med Genet. 1994. PMID: 8160730

2

Use of Y-chromosome-specific DNA probes to evaluate an XX male.

Farah SB, Garmes HM, Cavalcanti DP, Mello MP, Porrelli RN, Ramos CF, Sartorato EL. Farah SB, et al. Among authors: cavalcanti dp. Braz J Med Biol Res. 1991;24(2):149-56. Braz J Med Biol Res. 1991. PMID: 1823227

3

[Importance of the clinical genetics evaluation on hydrocephalus].

Wey-Vieira M, Cavalcanti DP, Lopes VL. Wey-Vieira M, et al. Among authors: cavalcanti dp. Arq Neuropsiquiatr. 2004 Jun;62(2B):480-6. doi: 10.1590/s0004-282x2004000300019. Epub 2004 Jul 20. Arq Neuropsiquiatr. 2004. PMID: 15273848 Free article. Portuguese.

4

Molecular findings in Brazilian patients with osteogenesis imperfecta.

Reis FC, Alexandrino F, Steiner CE, Norato DY, Cavalcanti DP, Sartorato EL. Reis FC, et al. Among authors: cavalcanti dp. J Appl Genet. 2005;46(1):105-8. J Appl Genet. 2005. PMID: 15741671

5

Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.

Jehee FS, Johnson D, Alonso LG, Cavalcanti DP, de Sá Moreira E, Alberto FL, Kok F, Kim C, Wall SA, Jabs EW, Boyadjiev SA, Wilkie AO, Passos-Bueno MR. Jehee FS, et al. Among authors: cavalcanti dp. Clin Genet. 2005 Jun;67(6):503-10. doi: 10.1111/j.1399-0004.2005.00438.x. Clin Genet. 2005. PMID: 15857417

6

Interphase-FISH study in three patients with tetraploid/diploid mosaicism.

Cavalcanti DP, Zanchetta LM. Cavalcanti DP, et al. Eur J Med Genet. 2005 Jan-Mar;48(1):41-50. doi: 10.1016/j.ejmg.2005.01.009. Epub 2005 Feb 1. Eur J Med Genet. 2005. PMID: 15953405

7

High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation.

Jehee FS, Krepischi-Santos AC, Rocha KM, Cavalcanti DP, Kim CA, Bertola DR, Alonso LG, D'Angelo CS, Mazzeu JF, Froyen G, Lugtenberg D, Vianna-Morgante AM, Rosenberg C, Passos-Bueno MR. Jehee FS, et al. Among authors: cavalcanti dp. J Med Genet. 2008 Jul;45(7):447-50. doi: 10.1136/jmg.2007.057042. Epub 2008 May 2. J Med Genet. 2008. PMID: 18456720

8

Unknown syndrome: abnormal facies, hypothyroidism, postaxial polydactyly, and severe retardation: a third patient.

Cavalcanti DP. Cavalcanti DP. J Med Genet. 1989 Dec;26(12):785-6. doi: 10.1136/jmg.26.12.785. J Med Genet. 1989. PMID: 2614801 Free PMC article.

9

Tetrasomy 9p caused by idic (9) (pter----q13----pter).

Cavalcanti DP, Ferrari I, de Almeida JC, de Pina Neto JM, de Oliveira JA. Cavalcanti DP, et al. Am J Med Genet. 1987 Jul;27(3):497-503. doi: 10.1002/ajmg.1320270303. Am J Med Genet. 1987. PMID: 3631125

10

Dandy-Walker malformation with postaxial polydactyly: further evidence for autosomal recessive inheritance.

Cavalcanti DP, Salomão MA. Cavalcanti DP, et al. Am J Med Genet. 1999 Jul 16;85(2):183-4. doi: 10.1002/(sici)1096-8628(19990716)85:2<183::aid-ajmg15>3.0.co;2-4. Am J Med Genet. 1999. PMID: 10406674

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