P Parvy - 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

P Parvy

Showing results (61-70 of 64) with videos related to

Pageof 7

Sort By:

You have reached the last page of results.This site can display upto 64 results.

Annales De Genetique|January 1, 1992

[Amino acids and trisomy 21]J Lejeune, M O Rethoré, M C de Blois, et al.

Journal of Inherited Metabolic Disease|January 1, 1989

Clinical approach to inherited metabolic diseases in the neonatal period: a 20-year surveyJ M Saudubray, H Ogier, J P Bonnefont, et al.

Journal of Inherited Metabolic Disease|August 1, 1998

Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?D Rabier, C Diry, A Rotig, et al.

European Journal of Pediatrics|March 1, 1996

Clinical outcome and long-term management of 17 patients with propionic acidaemiaS B van der Meer, F Poggi, M Spada, et al.

Pageof 7

Search research articles

Showing results (61-70 of 64) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 64 results.

Annales De Genetique|January 1, 1992

[Amino acids and trisomy 21]J Lejeune, M O Rethoré, M C de Blois, et al.

Journal of Inherited Metabolic Disease|January 1, 1989

Clinical approach to inherited metabolic diseases in the neonatal period: a 20-year surveyJ M Saudubray, H Ogier, J P Bonnefont, et al.

Journal of Inherited Metabolic Disease|August 1, 1998

Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?D Rabier, C Diry, A Rotig, et al.

European Journal of Pediatrics|March 1, 1996

Clinical outcome and long-term management of 17 patients with propionic acidaemiaS B van der Meer, F Poggi, M Spada, et al.

Pageof 7