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American Journal of Medical Genetics. Part A|September 27, 2006
Holoprosencephaly-like phenotype: clinical and genetic perspectivesA Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part A|September 27, 2006
Single maxillary central incisor, holoprosencephaly, and holoprosencephaly-like phenotypeA Richieri-Costa, Lucilene Arilho Ribeiro
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?Antonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and holoprosencephaly-like phenotypes: Review of facial and molecular findings in patients from a craniofacial hospital in BrazilAntonio Richieri-Costa, Lucilene Arilho Ribeiro
Brain & Development|September 11, 2007
Variable phenotypic manifestations of a K44N mutation in the TGIF geneAntonio Richieri-Costa, Lucilene Arilho Ribeiro
American Journal of Medical Genetics. Part A|September 27, 2006
PTCH mutations in four Brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRILucilene Arilho Ribeiro, Jeffrey C Murray, Antonio Richieri-Costa
American Journal of Medical Genetics. Part A|September 27, 2006
SIX3 mutations with holoprosencephalyLucilene Arilho Ribeiro, Kenia B El-Jaick, Maximilian Muenke, et al.
Brain & Development|April 29, 2009
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephalyClaudia Danielli Pereira Bertolacini, Antonio Richieri-Costa, Lucilene Arilho Ribeiro-Bicudo
American Journal of Medical Genetics. Part A|June 29, 2010
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: Report of four Brazilian patientsLucilene Arilho Ribeiro, Rodrigo Gonçalves Quiezi, Adriana Nascimento, et al.
Clinical Dysmorphology|March 4, 2011
A novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosisLucilene Arilho Ribeiro, Claudia Danielli Pereira Bertolacini, Rodrigo Gonçalves Quiezi, et al.
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