Guion-Almeida ML - Search Results

1

Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.

Richieri-Costa A, Guion-Almeida ML, Pagnan NA. Richieri-Costa A, et al. Am J Med Genet. 1992 Dec 1;44(6):800-2. doi: 10.1002/ajmg.1320440616. Am J Med Genet. 1992. PMID: 1481850

2

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

3

Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature.

Vendramini S, Richieri-Costa A, Guion-Almeida ML. Vendramini S, et al. Eur J Hum Genet. 2007 Apr;15(4):411-21. doi: 10.1038/sj.ejhg.5201770. Epub 2007 Feb 7. Eur J Hum Genet. 2007. PMID: 17290277 Review.

4

Pai syndrome: report of seven South American patients.

Guion-Almeida ML, Mellado C, Beltrán C, Richieri-Costa A. Guion-Almeida ML, et al. Am J Med Genet A. 2007 Dec 15;143A(24):3273-9. doi: 10.1002/ajmg.a.31962. Am J Med Genet A. 2007. PMID: 17907143

5

Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union.

Zechi-Ceide RM, Guion-Almeida ML, Zanchetta S, Richieri-Costa A. Zechi-Ceide RM, et al. Am J Med Genet A. 2007 Dec 15;143A(24):3295-301. doi: 10.1002/ajmg.a.32019. Am J Med Genet A. 2007. PMID: 17907157

6

Cerebro-oculo-nasal syndrome: 13 new Brazilian cases.

Guion-Almeida ML, Zechi-Ceide RM, Richieri-Costa A. Guion-Almeida ML, et al. Am J Med Genet A. 2007 Dec 15;143A(24):3252-66. doi: 10.1002/ajmg.a.32090. Am J Med Genet A. 2007. PMID: 17985375

7

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

8

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

9

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

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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