Guion-Almeida ML - Search Results

1

Mandibulofacial dysostosis Bauru type: Refining the phenotype.

Moura PP, Kokitsu-Nakata NM, Yatabe MS, Vendramini-Pittoli S, Hori PH, Guion-Almeida ML, Garib DG, Richieri-Costa A, Zechi-Ceide RM. Moura PP, et al. Among authors: guion almeida ml. Am J Med Genet A. 2017 Jul;173(7):1747-1753. doi: 10.1002/ajmg.a.38257. Epub 2017 May 30. Am J Med Genet A. 2017. PMID: 28558149

2

Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome.

Romanelli Tavares VL, Zechi-Ceide RM, Bertola DR, Gordon CT, Ferreira SG, Hsia GS, Yamamoto GL, Ezquina SA, Kokitsu-Nakata NM, Vendramini-Pittoli S, Freitas RS, Souza J, Raposo-Amaral CA, Zatz M, Amiel J, Guion-Almeida ML, Passos-Bueno MR. Romanelli Tavares VL, et al. Among authors: guion almeida ml. Am J Med Genet A. 2017 Apr;173(4):938-945. doi: 10.1002/ajmg.a.38101. Am J Med Genet A. 2017. PMID: 28328130

3

Auriculo-condylar syndrome: additional patients.

Guion-Almeida ML, Zechi-Ceide RM, Vendramini S, Kokitsu-Nakata NM. Guion-Almeida ML, et al. Am J Med Genet. 2002 Oct 1;112(2):209-14. doi: 10.1002/ajmg.10631. Am J Med Genet. 2002. PMID: 12244558

4

Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patients.

Guion-Almeida ML, Richieri-Costa A. Guion-Almeida ML, et al. Am J Med Genet A. 2009 May;149A(5):1006-11. doi: 10.1002/ajmg.a.32717. Am J Med Genet A. 2009. PMID: 19365836

5

Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes.

Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CD, Guion-Almeida ML, Richieri-Costa A. Zechi-Ceide RM, et al. Am J Med Genet A. 2009 Jun;149A(6):1277-9. doi: 10.1002/ajmg.a.32844. Am J Med Genet A. 2009. PMID: 19449411

6

Mandibulofacial syndrome with growth and mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome?

Guion-Almeida ML, Vendramini-Pittoli S, Passos-Bueno MR, Zechi-Ceide RM. Guion-Almeida ML, et al. Am J Med Genet A. 2009 Dec;149A(12):2762-4. doi: 10.1002/ajmg.a.32816. Am J Med Genet A. 2009. PMID: 19921636

7

Nonsyndromic alar clefts: report of five Brazilian patients.

Richieri-Costa A, Guion-Almeida ML. Richieri-Costa A, et al. Am J Med Genet A. 2009 Dec;149A(12):2765-7. doi: 10.1002/ajmg.a.32845. Am J Med Genet A. 2009. PMID: 19921637

8

Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: A new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome?

Zechi-Ceide RM, Guion-Almeida ML, Jehee FS, Rocha K, Passos-Bueno MR. Zechi-Ceide RM, et al. Am J Med Genet A. 2010 Jul;152A(7):1838-40. doi: 10.1002/ajmg.a.33477. Am J Med Genet A. 2010. PMID: 20583178

9

Frontonasal dysgenesis, first branchial arch anomalies, and pericallosal lipoma: A new subtype of frontonasal dysgenesis.

Guion-Almeida ML, Richieri-Costa A. Guion-Almeida ML, et al. Am J Med Genet A. 2010 Aug;152A(8):2039-42. doi: 10.1002/ajmg.a.33485. Am J Med Genet A. 2010. PMID: 20602490

10

Richieri-Costa-Pereira syndrome: a unique acrofacial dysostosis type. An overview of the Brazilian cases.

Favaro FP, Zechi-Ceide RM, Alvarez CW, Maximino LP, Antunes LF, Richieri-Costa A, Guion-Almeida ML. Favaro FP, et al. Am J Med Genet A. 2011 Feb;155A(2):322-31. doi: 10.1002/ajmg.a.33806. Epub 2010 Dec 22. Am J Med Genet A. 2011. PMID: 21271648 Review.

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