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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 cases
P P Mayock, P I Bader
Annals of Clinical Research
|
April 1, 1977
alpha1-Antitrypsin deficiency in clinic patients
R N Matzen, P I Bader, W D Block
Clinical Genetics
|
January 1, 1975
Vitiligo and dysgammaglobulinemia. A case report and family study
P I Bader, A Biegel, W W Epinette, et al.
Obstetrics and Gynecology
|
August 1, 1982
Müllerian agenesis, hypoplasia of distal extremities, unusual dermatoglyphics, and pigmentation
P I Bader, W R Keye, J T Cowan, et al.
Birth Defects Original Article Series
|
January 1, 1974
Inheritance of idiopathic nephrotic syndrome
P I Bader, J Grove, W E Nance, et al.
American Journal of Medical Genetics
|
December 23, 1999
Infantile refsum disease in four Amish sibs
P 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 biosynthesis
G 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 approach
E 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 aciduria
K M Gibson, J L Lohr, R L Broock, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
The American Journal of the Medical Sciences
|
March 1, 1979
Case report. Legionnaires' disease. A review of clinical aspects of 18 sporadic cases
P P Mayock, P I Bader
Annals of Clinical Research
|
April 1, 1977
alpha1-Antitrypsin deficiency in clinic patients
R N Matzen, P I Bader, W D Block
Clinical Genetics
|
January 1, 1975
Vitiligo and dysgammaglobulinemia. A case report and family study
P I Bader, A Biegel, W W Epinette, et al.
Obstetrics and Gynecology
|
August 1, 1982
Müllerian agenesis, hypoplasia of distal extremities, unusual dermatoglyphics, and pigmentation
P I Bader, W R Keye, J T Cowan, et al.
Birth Defects Original Article Series
|
January 1, 1974
Inheritance of idiopathic nephrotic syndrome
P I Bader, J Grove, W E Nance, et al.
American Journal of Medical Genetics
|
December 23, 1999
Infantile refsum disease in four Amish sibs
P 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 biosynthesis
G 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 approach
E 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 aciduria
K M Gibson, J L Lohr, R L Broock, et al.
Page
of 2