Author:
Tonomura Yasuyo,Hirano Makito,Shimada Keiji,Asai Hirohide,Ikeda Masanori,Kataoka Hiroshi,Tanaka Ichiro,Konishi Noboru,Ueno Satoshi
Subject
Neurology (clinical),General Medicine,Surgery
Reference17 articles.
1. Four cases of ‘retinitis pigmentosa’ occurring in the same family, and accompanied by general imperfections of development;Laurence;Br Ophthalmol Rev,1866
2. Geschwisterpaar mit adiposo-genitaler Dystrophie;Biedl;Dtsch Med Wochenschr,1922
3. Dystrophia adiposogenitalis, with atypical retinitis pigmentosa and mental deficiency—the Laurence–Biedl syndrome. A report of four cases in one family;Solis-Cohen;Am J Med Sci,1925
4. Identification of a novel BBS gene (BBS 12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Barfet–Biedl syndrome;Stoetzel;Am J Hum Genet,2007
5. New criteria for improved diagnosis of Bardet–Biedl syndrome: results of a population survey;Beales;J Med Genet,1999
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