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 A Phillips

Showing results (161-170 of 255) with videos related to

Pageof 26
Sort By:
Somatic Cell and Molecular Genetics|March 1, 1985
Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factorD C Riddell, R Mallonee, J A Phillips, et al.
The Johns Hopkins Medical Journal|August 1, 1979
Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab diseaseJ A Phillips, A F Scott, H H Kazazian, et al.
The Journal of Antimicrobial Chemotherapy|November 4, 2000
Use of mastalex to detect methicillin resistance in coagulase-negative staphylococciJ C Graham, J A Phillips, O M Murphy, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1990
Molecular analysis of autosomal dominant neurohypophyseal diabetes insipidusD R Repaske, J A Phillips, L T Kirby, et al.
American Journal of Human Genetics|October 1, 1991
Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elementsC D Bottema, R P Ketterling, S Ii, et al.
European Journal of Endocrinology|December 24, 1997
Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controlsJ K Wagner, A Eblé, J D Cogan, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 12, 2000
A novel mutation at the donor splice site of intron 3 of the GH-I gene in a patient with isolated growth hormone deficiencyY Hayashi, T Kamijo, M Yamamoto, et al.
Environmental Science & Technology|March 2, 2011
Increased mercury loadings to western Canadian alpine lakes over the past 150 yearsVanessa J A Phillips, Vincent L St Louis, Colin A Cooke, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the gene (GLCLC) that encodes the heavy subunit of gamma-glutamylcysteine synthetase to human chromosome 6E Sierra-Rivera, M L Summar, M Dasouki, et al.
American Journal of Clinical Pathology|September 1, 1989
Prenatal diagnosis of sickle cell anemia. Hemoglobin electrophoresis versus DNA analysisY F Posey, D Shah, J E Ulm, et al.
Pageof 26

Showing results (161-170 of 255) with videos related to

Sort By:
Pageof 26
Somatic Cell and Molecular Genetics|March 1, 1985
Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factorD C Riddell, R Mallonee, J A Phillips, et al.
The Johns Hopkins Medical Journal|August 1, 1979
Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab diseaseJ A Phillips, A F Scott, H H Kazazian, et al.
The Journal of Antimicrobial Chemotherapy|November 4, 2000
Use of mastalex to detect methicillin resistance in coagulase-negative staphylococciJ C Graham, J A Phillips, O M Murphy, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1990
Molecular analysis of autosomal dominant neurohypophyseal diabetes insipidusD R Repaske, J A Phillips, L T Kirby, et al.
American Journal of Human Genetics|October 1, 1991
Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elementsC D Bottema, R P Ketterling, S Ii, et al.
European Journal of Endocrinology|December 24, 1997
Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controlsJ K Wagner, A Eblé, J D Cogan, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 12, 2000
A novel mutation at the donor splice site of intron 3 of the GH-I gene in a patient with isolated growth hormone deficiencyY Hayashi, T Kamijo, M Yamamoto, et al.
Environmental Science & Technology|March 2, 2011
Increased mercury loadings to western Canadian alpine lakes over the past 150 yearsVanessa J A Phillips, Vincent L St Louis, Colin A Cooke, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the gene (GLCLC) that encodes the heavy subunit of gamma-glutamylcysteine synthetase to human chromosome 6E Sierra-Rivera, M L Summar, M Dasouki, et al.
American Journal of Clinical Pathology|September 1, 1989
Prenatal diagnosis of sickle cell anemia. Hemoglobin electrophoresis versus DNA analysisY F Posey, D Shah, J E Ulm, et al.
Pageof 26