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P I Bader

Showing results (11-20 of 23) with videos related to

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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 isolateP 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 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.
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 studyG 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 aciduriaK 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 syndromeJ 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 syndromeS 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 dysgenesisR 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 CGHS U Dhar, D del Gaudio, J R German, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|July 1, 1982
Lymphocyte capping in limb-girdle muscular dystrophy: patients and carriers in an Amish isolateP 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 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.
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 studyG 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 aciduriaK 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 syndromeJ 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 syndromeS 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 dysgenesisR 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 CGHS U Dhar, D del Gaudio, J R German, et al.
Pageof 3