I Baric - 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

I Baric

Showing results (11-20 of 14) with videos related to

Pageof 2

Sort By:

You have reached the last page of results.This site can display upto 14 results.

Neuropediatrics|November 5, 2003

Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamenS Kölker, G F Hoffmann, D S M Schor, et al.

Clinical Genetics|November 25, 2016

Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type IIL Dvorakova, H Vlaskova, A Sarajlija, et al.

Human Mutation|January 1, 1997

Frequency of RET mutations in long- and short-segment Hirschsprung diseaseM Seri, L Yin, V Barone, et al.

Human Molecular Genetics|September 5, 2001

The mutational spectrum of human malignant autosomal recessive osteopetrosisC Sobacchi, A Frattini, P Orchard, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Neuropediatrics|November 5, 2003

Clinical Genetics|November 25, 2016

Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type IIL Dvorakova, H Vlaskova, A Sarajlija, et al.

Human Mutation|January 1, 1997

Frequency of RET mutations in long- and short-segment Hirschsprung diseaseM Seri, L Yin, V Barone, et al.

Human Molecular Genetics|September 5, 2001

The mutational spectrum of human malignant autosomal recessive osteopetrosisC Sobacchi, A Frattini, P Orchard, et al.

Pageof 2