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W A Muir

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Clinical Genetics|August 1, 1977
An autosomal dominant midline cleft syndrome resembling familial holoprosencephalyA O Martin, J C Perrin, W A Muir, et al.
American Journal of Clinical Pathology|February 1, 1975
Hemochromatosis. Pathophysiologic and genetic considerationsC E Ross, W A Muir, B P Alan, et al.
The Journal of Clinical Investigation|October 1, 1984
Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigensW A Muir, S Hedrick, C A Alper, et al.
The Journal of Rheumatology. Supplement|January 1, 1977
HLA B27 in ankylosing spondylitis: differences in frequency and relative risk in American Blacks and CaucasiansM A Khan, W E Braun, I Kushner, et al.
Cancer Investigation|January 1, 1991
Protracted infusion of 5-FU with weekly low-dose cisplatin as second-line therapy in patients with metastatic colorectal cancer who have failed 5-FU monotherapyJ D Ahlgren, O Trocki, J J Gullo, et al.
The American Journal of Medicine|December 1, 1983
Arthritis of hemochromatosis. Clinical spectrum, relation to histocompatibility antigens, and effectiveness of early phlebotomyA D Askari, W A Muir, I A Rosner, et al.
Archives of Disease in Childhood|September 1, 1980
Maternal homocystinuria: studies of an untreated mother and fetusT W Kurczynski, W A Muir, L D Fleisher, et al.
American Journal of Medical Genetics|January 1, 1980
The recurrence risk for neural tube defects in the United States: a collaborative studyS Cowchock, E Ainbender, G Prescott, et al.
The New England Journal of Medicine|December 30, 1982
Magnetic-susceptibility measurement of human iron storesG M Brittenham, D E Farrell, J W Harris, et al.
The New England Journal of Medicine|April 26, 1979
Prenatal diagnosis of classic hemophiliaS I Firshein, L W Hoyer, J Lazarchick, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Clinical Genetics|August 1, 1977
An autosomal dominant midline cleft syndrome resembling familial holoprosencephalyA O Martin, J C Perrin, W A Muir, et al.
American Journal of Clinical Pathology|February 1, 1975
Hemochromatosis. Pathophysiologic and genetic considerationsC E Ross, W A Muir, B P Alan, et al.
The Journal of Clinical Investigation|October 1, 1984
Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigensW A Muir, S Hedrick, C A Alper, et al.
The Journal of Rheumatology. Supplement|January 1, 1977
HLA B27 in ankylosing spondylitis: differences in frequency and relative risk in American Blacks and CaucasiansM A Khan, W E Braun, I Kushner, et al.
Cancer Investigation|January 1, 1991
Protracted infusion of 5-FU with weekly low-dose cisplatin as second-line therapy in patients with metastatic colorectal cancer who have failed 5-FU monotherapyJ D Ahlgren, O Trocki, J J Gullo, et al.
The American Journal of Medicine|December 1, 1983
Arthritis of hemochromatosis. Clinical spectrum, relation to histocompatibility antigens, and effectiveness of early phlebotomyA D Askari, W A Muir, I A Rosner, et al.
Archives of Disease in Childhood|September 1, 1980
Maternal homocystinuria: studies of an untreated mother and fetusT W Kurczynski, W A Muir, L D Fleisher, et al.
American Journal of Medical Genetics|January 1, 1980
The recurrence risk for neural tube defects in the United States: a collaborative studyS Cowchock, E Ainbender, G Prescott, et al.
The New England Journal of Medicine|December 30, 1982
Magnetic-susceptibility measurement of human iron storesG M Brittenham, D E Farrell, J W Harris, et al.
The New England Journal of Medicine|April 26, 1979
Prenatal diagnosis of classic hemophiliaS I Firshein, L W Hoyer, J Lazarchick, et al.
Pageof 2