V. Bennouna Greene

Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly

Élise Schaefer, Ariane Zaloszyc, Julia Lauer et al. · Molecular Syndromology · 2010 · 78 citations · Full text

Primary Sdccag8 Mutations, Genetics, Renal Pathology +20

Sequence and Structure Requirements for Drosophila tRNA 5′- and 3′-End Processing

Louis Levinger, Vikram Vasisht, V. Bennouna Greene et al. · Journal of Biological Chemistry · 1995 · 37 citations · Full text

Confirmation of<i>ADAMTSL4</i>mutations for autosomal recessive isolated bilateral Ectopia Lentis

V. Bennouna Greene, Corinne Stoetzel, V. Pelletier et al. · Ophthalmic Genetics · 2010 · 36 citations

Ocular Disease, Developmental Biology, Adamts Proteases +11

Confirmation of <i>TFAP2A</i> gene involvement in branchio‐oculo‐facial syndrome (BOFS) and report of temporal bone anomalies

Corinne Stoetzel, S. Riehm, V. Bennouna Greene et al. · American Journal of Medical Genetics Part A · 2009 · 33 citations

Genetics, Branchio‐oculo‐facial Syndrome, Pathology +17