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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (6)
Showing records 1 to 6
Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia
Search within classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia12157 Combination of WAGR and Potocki-Shaffer contiguous deletion syndromes in a patient with an 11p11.2-p14 deletion
Bremond Gignac D; Crolla JA; Copin H; Guichet A; Bonneau D; Taine L; Lacombe D; Baumann C; Benzacken B; Verloes A
European Journal of Human Genetics 2005; 13: 409-413
12224 Characteristics of ocular pathological changes in familial congenital aniridia
Liu Y-Z; Cong R-C; Cui S-S; Ren G-C; Song S-J; Hou Z-Q; Hao Y-S; Ma Z-Z
International Journal of Ophthalmology 2005; 5: 291-293
12400 Aniridia and optic nerve hypoplasia
McCulley TJ; Mayer K; Dahr SS; Simpson J; Holland EJ
Eye 2005; 19: 762-764
12368 Implantation of iris devices in congenital and traumatic aniridias: surgery solutions and complications
Menezo JL; Martinez-Costa R; Cisneros A; Desco MC
European Journal of Ophthalmology 2005; 15: 451-457
12246 A case of novel de novo paired box gene 6 (PAX6) mutation with early-onset diabetes mellitus and aniridia
Nishi M; Sasahara M; Shono T; Saika S; Yamamoto Y; Ohkawa K; Furuta H; Nakao T; Sasaki H; Nanjo K
Diabetic Medicine 2005; 22: 641-644
12303 Aniridia associated with ptosis in three generations of the same family
Wammanda RD; Idris HW
Annals of Tropical Paediatrics 2005; 25: 59-62
