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TypeTitleAuthor(s)YearViews
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion
Journal:
American Journal of Medical Genetics, Part A
Publisher:
John Wiley & Sons, Inc.
Aldinger, KA; Kogan, J; Kimonis, V; Fernandez, B; Horn, D; Klopocki, E; Chung, B; Toutain, A; Weksberg, R; Millen, KJ; Barkovich, AJ; Dobyns, WB2013150
 
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)
Journal:
Clinical Dysmorphology
Publisher:
Lippincott Williams & Wilkins. The Journal's web site is located at http://www.lww.com/product/?0962-8827
Chung, BHY; Fernandez, B; Li, C; Chitayat, D2012171
 
Ulnar-Mammary syndrome: expending the phenotype to include ankyloglossia and cleft lip and palate
Proceedings/Conference:
Annual Meeting of the American Society of Human Genetics, ASHG 2010
Jessen, J; Chung, BHY; Fernandez, B; Li, C; Chitayat, D2010323
 
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