A E Fraley - 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

Filters

A E Fraley

Showing results (1-10 of 4) with videos related to

Pageof 1

Sort By:

Molecular Biology and Evolution|September 1, 1996

Mitochondrial mismatch analysis is insensitive to the mutational processA R Rogers, A E Fraley, M J Bamshad, et al.

Human Biology|February 1, 1996

mtDNA variation in caste populations of Andhra Pradesh, IndiaM Bamshad, A E Fraley, M H Crawford, et al.

American Journal of Human Genetics|September 1, 1995

Origins and affinities of modern humans: a comparison of mitochondrial and nuclear genetic dataL B Jorde, M J Bamshad, W S Watkins, et al.

American Journal of Human Genetics|March 3, 1999

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 geneP L Tavormina, G A Bellus, M K Webster, et al.

Pageof 1

Search research articles

Showing results (1-10 of 4) with videos related to

Sort By:

Pageof 1

Molecular Biology and Evolution|September 1, 1996

Mitochondrial mismatch analysis is insensitive to the mutational processA R Rogers, A E Fraley, M J Bamshad, et al.

Human Biology|February 1, 1996

mtDNA variation in caste populations of Andhra Pradesh, IndiaM Bamshad, A E Fraley, M H Crawford, et al.

American Journal of Human Genetics|September 1, 1995

Origins and affinities of modern humans: a comparison of mitochondrial and nuclear genetic dataL B Jorde, M J Bamshad, W S Watkins, et al.

American Journal of Human Genetics|March 3, 1999

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 geneP L Tavormina, G A Bellus, M K Webster, et al.

Pageof 1