Joseph H. Lee

Association of common variants, not rare mutations, in IRF6 With nonsyndromic clefts in a honduran population

G. Su, C. Flores, David T. Kent, 2011, The Laryngoscope.

Four New Families with Autosomal Dominant Partial Epilepsy with Auditory Features: Clinical Description and Linkage to Chromosome 10q24

W. Hauser, T. Gilliam, T. Pedley, 2002, Epilepsia.

Clinical Indicators of Genetic Susceptibility to Epilepsy

J. H. Lee, N. Risch, W. Hauser, 1996, Epilepsia.

Localization of a gene for partial epilepsy to chromosome 10q

N. Risch, W. Hauser, T. Pedley, 1995, Nature Genetics.

Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease

B. Vardarajan, C. Marquer, R. Nandakumar, 2023, EBioMedicine.

Novel IRF6 mutations in Honduran Van der Woude syndrome patients.

G. Su, C. Flores, A. Birkeland, 2011, Molecular medicine reports.

The association between interferon regulatory factor 6 (IRF6) and nonsyndromic cleft lip with or without cleft palate in a Honduran population

G. Su, C. Flores, Gillian R Diercks, 2009, The Laryngoscope.