Now showing items 1-4 of 4

A 5-base insertion in the γC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract

Ren, Zhaoxia; Shastry, Barker S.; Scott, Mark H.; Ayyagari, Radha; Padma, Tirunilai; Hejtmancik, J. Fielding; Parks, Marshall M.; Kaiser-Kupfer, Muriel I.; Li, Anren (Springer-Verlag, 2000-05)

(158.5KB)
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change

Hiriyanna, Kelaginamane T.; Bingham, Eve L.; Yashar, Beverly M.; Ayyagari, Radha; Fishman, Gerald A.; Small, Kent W.; Weinberg, David V.; Weleber, Richard G.; Lewis, Richard A.; Andreasson, Sten; Richards, Julia E.; Sieving, Paul A. (John Wiley & Sons, Inc., 1999-11)

(192.4KB)
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3–p21.2 between D1S2896 and D1S457 but outside ABCA4

Sabar, Farooq; Ayyagari, Radha; Fielding Hejtmancik, J.; Riazuddin, Sheikh; Sieving, Paul A.; Caruso, Raphael; Zhang, Qingjiong; Xiao, Xueshan; Amer Riazuddin, S.; Zulfiqar, Fareeha (Springer-Verlag, 2005-12)

(502.3KB)
Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy

Bingham, Eve L.; Sieving, Paul A.; Felius, Joost; Kemp, Jennifer; Szczesny, Janet J.; Kakuk, Laura E.; Ayyagari, Radha; Toda, Yumiko (Springer-Verlag, 2000-07)

(181.2KB)

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