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J M Killian

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American Journal of Medical Genetics|September 15, 1993

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletionR T Zori, J R Lupski, Z Heju, et al.

The American Journal of Medicine|March 10, 2001

Time trends in the prevalence of atherosclerosis: a population-based autopsy studyV L Roger, S A Weston, J M Killian, et al.

International Immunology|December 1, 2000

Aberrant T cell responses to myelin antigens during clinical exacerbation in patients with multiple sclerosisM V Tejada-Simon, Y C Zang, D Yang, et al.

Nature Genetics|October 1, 1993

Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, L Pentao, et al.

Cell|July 26, 1991

DNA duplication associated with Charcot-Marie-Tooth disease type 1AJ R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.

Neuron|September 1, 1996

Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelinationL E Warner, M J Hilz, S H Appel, et al.

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Search research articles

Showing results (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

American Journal of Medical Genetics|September 15, 1993

Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletionR T Zori, J R Lupski, Z Heju, et al.

The American Journal of Medicine|March 10, 2001

Time trends in the prevalence of atherosclerosis: a population-based autopsy studyV L Roger, S A Weston, J M Killian, et al.

International Immunology|December 1, 2000

Aberrant T cell responses to myelin antigens during clinical exacerbation in patients with multiple sclerosisM V Tejada-Simon, Y C Zang, D Yang, et al.

Nature Genetics|October 1, 1993

Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, L Pentao, et al.

Cell|July 26, 1991

DNA duplication associated with Charcot-Marie-Tooth disease type 1AJ R Lupski, R M de Oca-Luna, S Slaugenhaupt, et al.

Neuron|September 1, 1996

Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelinationL E Warner, M J Hilz, S H Appel, et al.

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