Pina-Neto JM - Search Results

1

A selective clinical cytogenetic study in prenatal and pediatric pathology: a comparison with unselected studies.

Pina-Neto JM, Ortolan D, Bitar VS, Mazzucatto LF, Fernandez HH, Peres LC. Pina-Neto JM, et al. Am J Med Genet A. 2008 Jun 1;146A(11):1497-501. doi: 10.1002/ajmg.a.32329. Am J Med Genet A. 2008. PMID: 18449928 No abstract available.

2

Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.

Piram A, Ortolan D, Peres LC, Pina-Neto JM, Riegel M, Schinzel A. Piram A, et al. Am J Med Genet A. 2003 Jul 15;120A(2):247-52. doi: 10.1002/ajmg.a.10004. Am J Med Genet A. 2003. PMID: 12833408 Review.

3

DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells.

Ribeiro CN, Peres LC, Pina-Neto JM. Ribeiro CN, et al. Braz J Med Biol Res. 2004 May;37(5):635-42. doi: 10.1590/s0100-879x2004000500002. Epub 2004 Apr 22. Braz J Med Biol Res. 2004. PMID: 15107923 Free article.

4

Somatic cytogenetic and azoospermia factor gene microdeletion studies in infertile men.

Pina-Neto JM, Carrara RC, Bisinella R, Mazzucatto LF, Martins MD, Sartoratto E, Yamasaki R. Pina-Neto JM, et al. Braz J Med Biol Res. 2006 Apr;39(4):555-61. doi: 10.1590/s0100-879x2006000400017. Epub 2006 Apr 3. Braz J Med Biol Res. 2006. PMID: 16612480 Free article.

5

De novo complex chromosome rearrangement: a study of two patients.

Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina-Neto JM. Melo DG, et al. Genet Couns. 2004;15(3):303-10. Genet Couns. 2004. PMID: 15517822

6

Raine dysplasia: a Brazilian case with a mild radiological involvement.

Acosta AX, Peres LC, Chimelli LC, Pina-Neto JM. Acosta AX, et al. Clin Dysmorphol. 2000 Apr;9(2):99-101. doi: 10.1097/00019605-200009020-00004. Clin Dysmorphol. 2000. PMID: 10826619

7

Caudal dysplasia sequence: severe phenotype presenting in offspring of patients with gestational and pregestational diabetes.

Versiani BR, Gilbert-Barness E, Giuliani LR, Peres LC, Pina-Neto JM. Versiani BR, et al. Clin Dysmorphol. 2004 Jan;13(1):1-5. doi: 10.1097/00019605-200401000-00001. Clin Dysmorphol. 2004. PMID: 15127755

8

De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.

Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina-Neto JM. Riegel M, et al. Genet Couns. 2001;12(1):69-75. Genet Couns. 2001. PMID: 11332980

9

Autosomal dominant atretic cephalocele with phenotype variability: report of a Brazilian family with six affected in four generations.

Carvalho DR, Giuliani LR, Simão GN, Santos AC, Pina-Neto JM. Carvalho DR, et al. Am J Med Genet A. 2006 Jul 1;140(13):1458-62. doi: 10.1002/ajmg.a.31255. Am J Med Genet A. 2006. PMID: 16718686

10

Noonan syndrome associated with unilateral iris coloboma and congenital chylothorax in an infant.

Carvalho DR, Alves VV, Minaré-Júnior A, Peres LC, Pina-Neto JM, Ramos ES. Carvalho DR, et al. Clin Dysmorphol. 2003 Apr;12(2):143-4. doi: 10.1097/00019605-200304000-00015. Clin Dysmorphol. 2003. PMID: 12868481

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