T. Mitchell

发表

A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.

P. Kramer, I. Maumenee, M. Litt, 1996, Genomics.

Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2.

P. Kramer, D. Schultz, I. Maumenee, 1997, Human molecular genetics.

The age-dependent deterioration in light touch sensation on the plantar aspect of the foot in a rural community in India: implications when screening for sensory impairment.

T. Mitchell, P. D. Mitchell, 2000, Leprosy review.

Colobomatous malformations of the eye.

I. Maumenee, T. Mitchell, 1990, Transactions of the American Ophthalmological Society.

Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts.

I. Maumenee, E. Lovrien, M. A. Lavery, 1990, American journal of medical genetics.

Genetic basis of total colourblindness among the Pingelapese islanders

I. Maumenee, Eduardo D. Silva, O. Sundin, 2000, Nature Genetics.

A novel locus for Leber congenital amaurosis maps to chromosome 6q.

I. Maumenee, J. Robitaille, A. Baffoe-Bonnie, 2000, American journal of human genetics.

Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome

S. Antonarakis, P. C. Huang, I. Maumenee, 1990, Human Genetics.

Inheritance of congenital esotropia.

T H Beaty, I H Maumenee, A Alston, 1986, Transactions of the American Ophthalmological Society.

Posterior Polar Cataract: Genetic Analysis of a Large Family

I. Maumenee, J. Sallum, O. Sundin, 2005, Ophthalmic genetics.