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American Journal of Medical Genetics
|
July 1, 1982
Lymphocyte capping in limb-girdle muscular dystrophy: patients and carriers in an Amish isolate
P I Bader, C J Bender, M T Creason, 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.
The Journal of the Indiana State Medical Association
|
July 1, 1981
The patient with mild to moderate essential hypertension: peripheral renin activity and a comparative drug study
G W Merkle, P I Bader, P L Creason, 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.
Nature
|
November 7, 1985
Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome
J F Gusella, R E Tanzi, P I Bader, et al.
Clinical Genetics
|
June 30, 2009
Identification of critical regions for clinical features of distal 10q deletion syndrome
S A Yatsenko, M C Kruer, P I Bader, et al.
Cytogenetic and Genome Research
|
June 26, 2004
Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesis
R Sood, P I Bader, M C Speer, et al.
American Journal of Medical Genetics. Part A
|
February 27, 2010
22q13.3 deletion syndrome: clinical and molecular analysis using array CGH
S U Dhar, D del Gaudio, J R German, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
July 1, 1982
Lymphocyte capping in limb-girdle muscular dystrophy: patients and carriers in an Amish isolate
P I Bader, C J Bender, M T Creason, 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.
The Journal of the Indiana State Medical Association
|
July 1, 1981
The patient with mild to moderate essential hypertension: peripheral renin activity and a comparative drug study
G W Merkle, P I Bader, P L Creason, 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.
Nature
|
November 7, 1985
Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome
J F Gusella, R E Tanzi, P I Bader, et al.
Clinical Genetics
|
June 30, 2009
Identification of critical regions for clinical features of distal 10q deletion syndrome
S A Yatsenko, M C Kruer, P I Bader, et al.
Cytogenetic and Genome Research
|
June 26, 2004
Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesis
R Sood, P I Bader, M C Speer, et al.
American Journal of Medical Genetics. Part A
|
February 27, 2010
22q13.3 deletion syndrome: clinical and molecular analysis using array CGH
S U Dhar, D del Gaudio, J R German, et al.
Page
of 3