Susan H. Blanton

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

S. Daiger, S. Blanton, J. Heckenlively, 1991, Genomics.

Evidence for craniofacial enhancer variation underlying nonsyndromic cleft lip and palate

J. Mulliken, S. Blanton, W. J. Zheng, 2020, Human Genetics.

Studies of TBX4 and chromosome 17q23.1q23.2: An uncommon cause of nonsyndromic clubfoot

N. Ahituv, C. Bacino, J. Vandermeer, 2012, American journal of medical genetics. Part A.

Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families.

C. Amos, J. Mulliken, R. Winter, 1995, American journal of human genetics.

North Carolina Macular Dystrophy (mcdr1) Caused by a Novel Tandem Duplication of the Prdm13 Gene Retina Foundation of the Southwest Recommended Citation

D. Koboldt, L. Sullivan, K. Locke, 2022 .

Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors.

S. Daiger, S. Blanton, L. Sadler, 1992, Genomics.

Cleft lip and palate: no evidence of linkage to transforming growth factor alpha.

S. Daiger, S. Blanton, J. Hecht, 1991, American journal of human genetics.