M S Tanner - 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

M S Tanner

Showing results (91-100 of 94) with videos related to

Pageof 10

Sort By:

You have reached the last page of results.This site can display upto 94 results.

Journal of Inherited Metabolic Disease|March 10, 1999

Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type IIN J Manning, J R Bonham, M Downing, et al.

Journal of Inherited Metabolic Disease|May 11, 1999

The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial diseaseJ R Bonham, P Guthrie, M Downing, et al.

Journal of Inherited Metabolic Disease|April 5, 2001

Features of carnitine palmitoyltransferase type I deficiencyS E Olpin, J Allen, J R Bonham, et al.

Nature Genetics|November 7, 1998

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasisS S Strautnieks, L N Bull, A S Knisely, et al.

Pageof 10

Search research articles

Showing results (91-100 of 94) with videos related to

Sort By:

Pageof 10

You have reached the last page of results.This site can display upto 94 results.

Journal of Inherited Metabolic Disease|March 10, 1999

Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type IIN J Manning, J R Bonham, M Downing, et al.

Journal of Inherited Metabolic Disease|May 11, 1999

The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial diseaseJ R Bonham, P Guthrie, M Downing, et al.

Journal of Inherited Metabolic Disease|April 5, 2001

Features of carnitine palmitoyltransferase type I deficiencyS E Olpin, J Allen, J R Bonham, et al.

Nature Genetics|November 7, 1998

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasisS S Strautnieks, L N Bull, A S Knisely, et al.

Pageof 10