R. Lin

Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome

R. Kucherlapati, C. Seidman, Craig T. Basson1, 1997, Nature Genetics.

Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations.

J. Seidman, S. Weremowicz, R. Bruzzone, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Erratum: Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome

J. Seidman, R. Kucherlapati, C. Seidman, 1997, Nature Genetics.

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

J. Seidman, B. Bruneau, M. Bamshad, 1997, Nature Genetics.

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

J. Seidman, R. Kucherlapati, C. Seidman, 1997, Nature genetics.

A family showing inheritance of the Inab phenotype

R. Lin, J. Herman, G. L. Daniels, 1988, Transfusion.

The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.

J. Seidman, M. Bamshad, L. Jorde, 1999, American journal of human genetics.

Mutations in human TBX3 alter limb, apocrine, and genital development in ulnar-mammary syndrome

J. Seidman, B. Bruneau, M. Bamshad, 1998, Nature Genetics.