| Literature DB >> 20358606 |
Gülen Eda Utine1, Jeroen Breckpot, Bernard Thienpont, Yasemin Alanay, Cemalettin Aksoy, Koray Boduroğlu, Koenraad Devriendt.
Abstract
In 1989, Tsukahara and colleagues described a single female with a provisionally unique pattern of malformation consisting of low intelligence, short stature, brachydactyly type A1, and characteristic facial features. We report on a second patient confirming Tsukahara syndrome as an established entity. (c) 2010 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2010 PMID: 20358606 DOI: 10.1002/ajmg.a.33325
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802