Results 1 to 3 of 3
Page 1 of 1
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion
American Journal of Medical Genetics, Part A
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, WB2013170
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)
Clinical Dysmorphology
Lippincott Williams & Wilkins. The Journal's web site is located at
Chung, BHY; Fernandez, B; Li, C; Chitayat, D2012187
Ulnar-Mammary syndrome: expending the phenotype to include ankyloglossia and cleft lip and palate
Annual Meeting of the American Society of Human Genetics, ASHG 2010
Jessen, J; Chung, BHY; Fernandez, B; Li, C; Chitayat, D2010346
Page 1 of 1
Export Records
Step 1: Select content and export format
  • Citation only
Step 2: Select export method
  • Download