Browse by Author Fernandez, B
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| Title | Author(s) | Year | View Count |
 | Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion | Aldinger, KA; Kogan, J; Kimonis, V; Fernandez, B; Horn, D; Klopocki, E; Chung, B; Toutain, A; Weksberg, R; Millen, KJ; Barkovich, AJ; Dobyns, WB | 2013 | 42 |
 | Correspondence: further studies on a kindred reported by Li 2009 as ‘A new syndrome of ankyloglossia and ulnar ray defects in Newfoundland kindred’. From ‘new syndrome’ through EEC to ulnar mammary syndrome (Letter to the Editor) | Chung, BHY; Fernandez, B; Li, C; Chitayat, D | 2012 | 92 |
| Ulnar-Mammary syndrome: expending the phenotype to include ankyloglossia and cleft lip and palate | Jessen, J; Chung, BHY; Fernandez, B; Li, C; Chitayat, D | 2010 | 157 |
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