Author:
Sharma Vishakha M.,Ruiz de Luzuriaga Arlene M.,Waggoner Darrel,Greenwald Mark,Stein Sarah L.
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Reference28 articles.
1. Two 46, XX,t(X;Y) females with linear skin defects and congenital micropthalmia: a new syndrome at Xp22.3;Al-Gazali;J Med Genet,1990
2. Midas syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome;Happle;Am J Med Genet,1993
3. Xp22.3 microdeletion in a 19-year-old girl with clinical features of MLS syndrome;Enright;Pediatr Dermatol,2003
4. Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22;Zvulunov;Br J Dermatol,1998
5. Phenotypic variation in ophthalmic manifestations of MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea);Cape;Arch Ophthalmol,2004
Cited by
24 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献