kw.\*:("Oculoauriculovertebral spectrum")
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2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate geneROORYCK, Caroline; STEF, Marianne; BURGELIN, Ingrid et al.European journal of medical genetics. 2009, Vol 52, Num 6, pp 446-449, issn 1769-7212, 4 p.Article
Humoral Immune Deficiency and Hemifacial Microsomia Seen in One FamilyMIKHAK, Zamaneh; MULLIKEN, John B; LEE, John et al.The Cleft palate-craniofacial journal. 2009, Vol 46, Num 5, pp 477-480, issn 1055-6656, 4 p.Article
Branchiootorenal Syndrome and Oculoauriculovertebral Spectrum Features Associated With Duplication of SIX1, SIX6, and OTX2 Resulting From a Complex Chromosomal RearrangementZHISHUO OU; MARTIN, Donna M; BEDOYAN, Jirair K et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 19, pp 2480-2489, issn 1552-4825, 10 p.Article
Macrostomia, preauricular tags, and external ophthalmoplegia : A new autosomal dominant syndrome within the oculoauriculovertebral spectrum?RICHIERI-COSTA, Antonio; ARILHO RIBEIRO, Lucilene.The Cleft palate-craniofacial journal. 2006, Vol 43, Num 4, pp 429-434, issn 1055-6656, 6 p.Article
Oculoauriculovertebral spectrum with radial defects : a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literatureVENDRARMINI, Siulan; RICHIERI-COSTA, Antonio; GUION-ALMEIDA, Maria Leine et al.European journal of human genetics. 2007, Vol 15, Num 4, pp 411-421, issn 1018-4813, 11 p.Article