Richieri-Costa A - Search Results

1

Tooth abnormalities and soft tissue alterations in patients with G/BBB syndrome.

da Silva Dalben G, Richieri-Costa A, de Assis Taveira LA. da Silva Dalben G, et al. Oral Dis. 2008 Nov;14(8):747-53. doi: 10.1111/j.1601-0825.2008.01457.x. Epub 2008 Jun 21. Oral Dis. 2008. PMID: 18627501

2

Tooth abnormalities and soft tissue changes in patients with velocardiofacial syndrome.

da Silva Dalben G, Richieri-Costa A, de Assis Taveira LA. da Silva Dalben G, et al. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008 Aug;106(2):e46-51. doi: 10.1016/j.tripleo.2008.04.019. Epub 2008 Jun 13. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008. PMID: 18554940

3

Dental anomalies in Richieri-Costa-Pereira syndrome.

Severini JM, da Silva Dalben G, Richieri-Costa A, Ozawa TO. Severini JM, et al. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Jul;114(1):99-106. doi: 10.1016/j.oooo.2012.03.009. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012. PMID: 22727098

4

Craniofacial Morphology in Patients With Opitz G/BBB Syndrome.

Dalben GDS, Garib DG, Pinto RO, Richieri-Costa A, Taveira LAA. Dalben GDS, et al. Among authors: richieri costa a. Cleft Palate Craniofac J. 2019 Nov;56(10):1366-1372. doi: 10.1177/1055665619857001. Epub 2019 Jun 19. Cleft Palate Craniofac J. 2019. PMID: 31216877

5

Craniofacial morphology in patients with velocardiofacial syndrome.

Dalben Gda S, Richieri-Costa A, Taveira LA. Dalben Gda S, et al. Cleft Palate Craniofac J. 2010 May;47(3):241-6. doi: 10.1597/08-278.1. Cleft Palate Craniofac J. 2010. PMID: 20426673

6

Clinical evaluation and COL2A1 gene analysis in 21 Brazilian families with Stickler syndrome: identification of novel mutations, further genotype/phenotype correlation, and its implications for the diagnosis.

Zechi-Ceide RM, Jesus Oliveira NA, Guion-Almeida ML, Antunes LF, Richieri-Costa A, Passos-Bueno MR. Zechi-Ceide RM, et al. Eur J Med Genet. 2008 May-Jun;51(3):183-96. doi: 10.1016/j.ejmg.2007.12.008. Epub 2008 Jan 9. Eur J Med Genet. 2008. PMID: 18276201

7

Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement.

Alvarez CW, Guion-Almeida ML, Richieri-Costa A. Alvarez CW, et al. J Craniomaxillofac Surg. 2014 Dec;42(8):1952-7. doi: 10.1016/j.jcms.2014.08.007. Epub 2014 Sep 7. J Craniomaxillofac Surg. 2014. PMID: 25441864

8

Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: a possible "new" autosomal recessive syndrome?

Guion-Almeida ML, Richieri-Costa A. Guion-Almeida ML, et al. Am J Med Genet A. 2006 Nov 15;140(22):2478-81. doi: 10.1002/ajmg.a.31518. Am J Med Genet A. 2006. PMID: 17041938

9

Clinical findings in patients with GLI2 mutations--phenotypic variability.

Bertolacini CD, Ribeiro-Bicudo LA, Petrin A, Richieri-Costa A, Murray JC. Bertolacini CD, et al. Clin Genet. 2012 Jan;81(1):70-5. doi: 10.1111/j.1399-0004.2010.01606.x. Epub 2011 Jan 19. Clin Genet. 2012. PMID: 21204792 Free PMC article.

10

About Cuddapah et al. Paper Entitled "IRF6 Sequencing in Interrupted Clefting".

Alvarez CW, Guion-Almeida ML, Richieri-Costa A. Alvarez CW, et al. Cleft Palate Craniofac J. 2017 Jul;54(4):494. doi: 10.1597/16-161. Epub 2016 Jul 21. Cleft Palate Craniofac J. 2017. PMID: 27441701 No abstract available.

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