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P I Bader

Showing results (1-10 of 17) with videos related to

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The American Journal of the Medical Sciences|March 1, 1979
Case report. Legionnaires' disease. A review of clinical aspects of 18 sporadic casesP P Mayock, P I Bader
Annals of Clinical Research|April 1, 1977
alpha1-Antitrypsin deficiency in clinic patientsR N Matzen, P I Bader, W D Block
Clinical Genetics|January 1, 1975
Vitiligo and dysgammaglobulinemia. A case report and family studyP I Bader, A Biegel, W W Epinette, et al.
Obstetrics and Gynecology|August 1, 1982
Müllerian agenesis, hypoplasia of distal extremities, unusual dermatoglyphics, and pigmentationP I Bader, W R Keye, J T Cowan, et al.
Birth Defects Original Article Series|January 1, 1974
Inheritance of idiopathic nephrotic syndromeP I Bader, J Grove, W E Nance, et al.
American Journal of Medical Genetics|December 23, 1999
Infantile refsum disease in four Amish sibsP I Bader, S Dougherty, N Cangany, et al.
American Journal of Medical Genetics|September 1, 1984
Brief clinical report: neural tube defects in dup(11q)P I Bader, S M Haney, R A Munsick, et al.
The New England Journal of Medicine|June 19, 1986
Mevalonic aciduria--an inborn error of cholesterol and nonsterol isoprene biosynthesisG Hoffmann, K M Gibson, I K Brandt, et al.
The Journal of Pediatrics|August 7, 2001
The subtle facial signs of prenatal exposure to alcohol: an anthropometric approachE S Moore, R E Ward, P L Jamison, et al.
Enzyme|January 1, 1989
Mevalonate kinase in lysates of cultured human fibroblasts and lymphoblasts: kinetic properties, assay conditions, carrier detection and measurement of residual activity in a patient with mevalonic aciduriaK M Gibson, J L Lohr, R L Broock, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
The American Journal of the Medical Sciences|March 1, 1979
Case report. Legionnaires' disease. A review of clinical aspects of 18 sporadic casesP P Mayock, P I Bader
Annals of Clinical Research|April 1, 1977
alpha1-Antitrypsin deficiency in clinic patientsR N Matzen, P I Bader, W D Block
Clinical Genetics|January 1, 1975
Vitiligo and dysgammaglobulinemia. A case report and family studyP I Bader, A Biegel, W W Epinette, et al.
Obstetrics and Gynecology|August 1, 1982
Müllerian agenesis, hypoplasia of distal extremities, unusual dermatoglyphics, and pigmentationP I Bader, W R Keye, J T Cowan, et al.
Birth Defects Original Article Series|January 1, 1974
Inheritance of idiopathic nephrotic syndromeP I Bader, J Grove, W E Nance, et al.
American Journal of Medical Genetics|December 23, 1999
Infantile refsum disease in four Amish sibsP I Bader, S Dougherty, N Cangany, et al.
American Journal of Medical Genetics|September 1, 1984
Brief clinical report: neural tube defects in dup(11q)P I Bader, S M Haney, R A Munsick, et al.
The New England Journal of Medicine|June 19, 1986
Mevalonic aciduria--an inborn error of cholesterol and nonsterol isoprene biosynthesisG Hoffmann, K M Gibson, I K Brandt, et al.
The Journal of Pediatrics|August 7, 2001
The subtle facial signs of prenatal exposure to alcohol: an anthropometric approachE S Moore, R E Ward, P L Jamison, et al.
Enzyme|January 1, 1989
Mevalonate kinase in lysates of cultured human fibroblasts and lymphoblasts: kinetic properties, assay conditions, carrier detection and measurement of residual activity in a patient with mevalonic aciduriaK M Gibson, J L Lohr, R L Broock, et al.
Pageof 2