L Ala-Kokko - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

L Ala-Kokko

Showing results (81-90 of 85) with videos related to

Pageof 9

Sort By:

You have reached the last page of results.This site can display upto 85 results.

European Journal of Human Genetics : EJHG|October 22, 1998

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.

Journal of Medical Genetics|January 16, 2007

Phenotypic and population differences in the association between CILP and lumbar disc diseaseI M Virtanen, Y Q Song, K M C Cheung, et al.

American Journal of Human Genetics|November 1, 1996

Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16G Tromp, H Kuivaniemi, S Raphael, et al.

Immunology|January 20, 1999

Characterization of recombinant type II collagen: arthritogenicity and tolerogenicity in DBA/1 miceL K Myers, D D Brand, X J Ye, et al.

American Journal of Human Genetics|September 16, 1999

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.

Pageof 9

Search research articles

Showing results (81-90 of 85) with videos related to

Sort By:

Pageof 9

You have reached the last page of results.This site can display upto 85 results.

European Journal of Human Genetics : EJHG|October 22, 1998

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.

Journal of Medical Genetics|January 16, 2007

Phenotypic and population differences in the association between CILP and lumbar disc diseaseI M Virtanen, Y Q Song, K M C Cheung, et al.

American Journal of Human Genetics|November 1, 1996

Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16G Tromp, H Kuivaniemi, S Raphael, et al.

Immunology|January 20, 1999

Characterization of recombinant type II collagen: arthritogenicity and tolerogenicity in DBA/1 miceL K Myers, D D Brand, X J Ye, et al.

American Journal of Human Genetics|September 16, 1999

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.

Pageof 9