T. Levi

发表

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

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

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 the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

J. Seidman, E. Brown, C. Seidman, 1993, Cell.

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

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

Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13

C. L. Jackson, M. Shemesh, T. Levi, 2001, European Journal of Human Genetics.

Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog.

N. Copeland, D. Gilbert, N. Jenkins, 1995, Genomics.

Cloning and characterization of a novel human gene RNF38 encoding a conserved putative protein with a RING finger domain.

Tamar Kahan, T. Levi, S. Mitrani‐Rosenbaum, 2002, Biochemical and biophysical research communications.

Fine-structure mapping of the hereditary inclusion body myopathy locus.

C. L. Jackson, C. Thiel, E. Tiram, 1999, Genomics.

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.

J. Seidman, H. Watkins, C. Seidman, 1992, The New England journal of medicine.

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.

S. Solomon, J. Seidman, R. Holcombe, 1989, The New England journal of medicine.

Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog.

N. Copeland, D. Gilbert, C. Seidman, 1995, Genomics.

Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome.

J. Seidman, C. Tabin, B. Bruneau, 1999, Developmental biology.