Guion-Almeida ML - Search Results

1

Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients.

Guion-Almeida ML, Zechi-Ceide RM, Richieri-Costa A. Guion-Almeida ML, et al. Am J Med Genet. 1999 Nov 5;87(1):72-7. doi: 10.1002/(sici)1096-8628(19991105)87:1<72::aid-ajmg15>3.0.co;2-7. Am J Med Genet. 1999. PMID: 10528252

2

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

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

Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?

Guion-Almeida ML, Machado-Paula LA, Richieri-Costa A. Guion-Almeida ML, et al. Am J Med Genet A. 2004 Aug 30;129A(2):156-61. doi: 10.1002/ajmg.a.30153. Am J Med Genet A. 2004. PMID: 15316972

5

A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate.

Guion-Almeida ML, Zechi-Ceide RM, Vendramini S, Ju Nior AT. Guion-Almeida ML, et al. Clin Dysmorphol. 2006 Jul;15(3):171-174. doi: 10.1097/01.mcd.0000220603.09661.7e. Clin Dysmorphol. 2006. PMID: 16760738

6

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

7

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.

8

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

9

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

10

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

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