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3.4.1 Linkage studies (3)

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21027 Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma
Pasutto F; Krumbiegel M; Mardin CY; Paoli D; Lämmer R; Weber BH; Kruse FE; Schlötzer-Schrehardt U; Reis A
Investigative Ophthalmology and Visual Science 2008; 49: 1459-1463
21214 Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort
Yang X; Zabriskie NA; Hau VS; Chen H; Tong Z; Gibbs D; Farhi P; Katz BJ; Luo L; Pearson E
Cell Cycle 2008; 7: 521-524
21299 Clinical evaluation and COL2A1 gene analysis in 21 Brazilian families with Stickler syndrome: Identification of novel mutations, further genotype/phenotype correlation, and its implications for the diagnosis
Zechi-Ceide RM; Jesus Oliveira NA; Guion-Almeida ML; Antunes LFBB; Richieri-Costa A; Passos-Bueno MRS
European Journal of Medical Genetics 2008; 51: 183-196

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