Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J W Mace

Showing results (11-20 of 33) with videos related to

Pageof 4
Sort By:
Lancet (London, England)|March 27, 1971
Raised nyctohemeral (night and day) growth hormone: levels in conditions with primordial short statureR W Gotlin, J W Mace, H K Silver
JAMA|July 13, 1970
Erythroderma and erythroblastosis feralisJ E Schanberger, M D Cunningham, J W Mace
Military Medicine|November 1, 1970
Some postnatal aspects of intrauterine transfusionsM D Cunningham, J W Mace, J E Schanberger
Blood|April 1, 1980
Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression testR Carmel, A A Bedros, J W Mace, et al.
Clinical Genetics|January 1, 1973
Antenatal diagnosis of argininosuccinic aciduriaS I Goodman, J W Mace, B Turner, et al.
Clinical Pediatrics|January 1, 1976
The child with an unusual odor. A clinical resuméJ W Mace, S I Goodman, W R Centerwall, et al.
American Journal of Diseases of Children (1960)|March 1, 1972
The 4p-syndromeJ W Mace, M D Cunningham, D W Smith, et al.
Pediatric Research|January 1, 1980
Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoproteinS I Goodman, E R McCabe, P V Fennessey, et al.
American Journal of Diseases of Children (1960)|September 1, 1971
Congenital hereditary nonprogressive external ophthalmoplegiaJ W Mace, H D Sponaugle, R Y Mitsunaga, et al.
The Journal of Pediatrics|May 1, 1971
Partial deletion of short arm of chromosome no. 4J W Mace, M D Cunningham, O J Miller, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Lancet (London, England)|March 27, 1971
Raised nyctohemeral (night and day) growth hormone: levels in conditions with primordial short statureR W Gotlin, J W Mace, H K Silver
JAMA|July 13, 1970
Erythroderma and erythroblastosis feralisJ E Schanberger, M D Cunningham, J W Mace
Military Medicine|November 1, 1970
Some postnatal aspects of intrauterine transfusionsM D Cunningham, J W Mace, J E Schanberger
Blood|April 1, 1980
Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression testR Carmel, A A Bedros, J W Mace, et al.
Clinical Genetics|January 1, 1973
Antenatal diagnosis of argininosuccinic aciduriaS I Goodman, J W Mace, B Turner, et al.
Clinical Pediatrics|January 1, 1976
The child with an unusual odor. A clinical resuméJ W Mace, S I Goodman, W R Centerwall, et al.
American Journal of Diseases of Children (1960)|March 1, 1972
The 4p-syndromeJ W Mace, M D Cunningham, D W Smith, et al.
Pediatric Research|January 1, 1980
Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoproteinS I Goodman, E R McCabe, P V Fennessey, et al.
American Journal of Diseases of Children (1960)|September 1, 1971
Congenital hereditary nonprogressive external ophthalmoplegiaJ W Mace, H D Sponaugle, R Y Mitsunaga, et al.
The Journal of Pediatrics|May 1, 1971
Partial deletion of short arm of chromosome no. 4J W Mace, M D Cunningham, O J Miller, et al.
Pageof 4