The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle von D'Alessandro, Lisa C.A., Latney, Brande C., Paluru, Prasuna C., Goldmuntz, Elizabeth

Volltext

Identification of a Novel Locus on 2q for Autosomal Dominant High-Grade Myopia von Paluru, Prasuna C, Nallasamy, Sudha, Devoto, Marcella, Rappaport, Eric F, Young, Terri L

Volltext

Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota von Nallasamy, Sudha, Paluru, Prasuna C, Devoto, Marcella, Wasserman, Nora F, Zhou, Jie, Young, Terri L

Volltext

Sequence variants in the transforming growth β-induced factor (TGIF) gene are not associated with high myopia von SCAVELLO, Genaro S, PALURU, Prasuna C, GANTER, William R, YOUNG, Terri L

Volltext

Exclusion of lumican and fibromodulin as candidate genes in MYP3 linked high grade myopia von Paluru, Prasuna C, Scavello, Genaro S, Ganter, William R, Young, Terri L

Volltext

Microarray analysis of gene expression in human donor sclera von Young, Terri L, Scavello, Genaro S, Paluru, Prasuna C, Choi, Jonathan D, Rappaport, Eric F, Rada, Jody A

Volltext

Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes von Scavello, Jr, Genaro S, Paluru, Prasuna C, Zhou, Jie, White, Peter S, Rappaport, Eric F, Young, Terri L

Volltext

Abstract 17979: A Subset of Patients with Isolated Transposition of the Great Arteries and Double Outlet Right Ventricle Fall Within the Spectrum of Heterotaxy Syndrome von D'Alessandro, Lisa C, Latney, Brande C, Paluru, Prasuna C, Goldmuntz, Elizabeth

Volltext

X-Linked High Myopia Associated With Cone Dysfunction von Young, Terri L, Deeb, Samir S, Ronan, Shawn M, Dewan, Andrew T, Alvear, Alison B, Scavello, Genaro S, Paluru, Prasuna C, Brott, Marcia S, Hayashi, Takaaki, Holleschau, Ann M, Benegas, Nancy, Schwartz, Marianne, Atwood, Larry D, Oetting, William S, Rosenberg, Thomas, Motulsky, Arno G, King, Richard A

Volltext

Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity von Hutcheson, Kelly A, Paluru, Prasuna C, Bernstein, Steven L, Koh, Jamie, Rappaport, Eric F, Leach, Richard A, Young, Terri L

Volltext

Sequence Variants in the Transforming Growth {beta}-Induced Factor (TGIF) Gene Are Not Associated with High Myopia von Scavello, Genaro S, Paluru, Prasuna C, Ganter, William R, Young, Terri L

Volltext

New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17 von Paluru, Prasuna, Ronan, Shawn M, Heon, Elise, Devoto, Marcella, Wildenberg, Scott C, Scavello, Genaro, Holleschau, Ann, Makitie, Outi, Cole, William G, King, Richard A, Young, Terri L

Volltext