Mutations in human cause limb and cardiac malformation in Holt-Oram syndromeCraig T. Basson, Christine E. Seidman, Seidman J.G et al.|Nature Genetics|1997Cited by 1.1k
Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidismMartin R. Pollak, Jonathan G. Seidman, Edward M. Brown et al.|Cell|1993Cited by 1.1k
Characteristics and Prognostic Implications of Myosin Missense Mutations in Familial Hypertrophic CardiomyopathyHugh Watkins, J G Seidman, Anthony Rosenzweig et al.|New England Journal of Medicine|1992Cited by 746
Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1John A. Jarcho, Christine E. Seidman, William J. McKenna et al.|New England Journal of Medicine|1989Cited by 540
Cloning, Expression, and Chromosomal Location of SHH and IHH: Two Human Homologues of the Drosophila Segment Polarity Gene HedgehogValeria Marigo, Cliff Tabin, Drucilla J. Roberts et al.|Genomics|1995Cited by 192