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F R Goodman

Showing results (31-40 of 52) with videos related to

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Clinical Genetics|April 3, 1999
Preaxial polydactyly in an infant with Down's syndromeA V Ramanan, K Hussain, S T Kempley, et al.
Clinical Genetics|March 22, 2001
Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLINC Bacchelli, F R Goodman, P J Scambler, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1993
How often should we measure the urinary anion gap for cases of suspected renal tubular acidosis?C P Streather, A O Phillips, F R Goodman, et al.
Circulation Research|November 1, 1972
Effects of added or substituted potassium ion on 45 Ca movements in rabbit aortic smooth muscleF R Goodman, G B Weiss, M N Weinberg, et al.
Prenatal Diagnosis|January 22, 2005
Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locusE K Bijlsma, A C Knegt, C M Bilardo, et al.
Journal of Cardiovascular Pharmacology|March 1, 1979
Effects of hypertonic mannitol on contractile responses and 45Ca movements in isolated canine arteriesF R Goodman, J T Willerson, R K Hester, et al.
Clinical and Experimental Hypertension. Part A, Theory and Practice|January 1, 1987
Central and peripheral inhibition of angiotensin converting enzyme (ACE) in the SHR: correlation with the antihypertensive activity of ACE inhibitorsJ A Norman, M Lehmann, F R Goodman, et al.
Clinical Genetics|August 16, 2003
ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndromeC Bacchelli, L C Wilson, J A Cook, et al.
Journal of Medicinal Chemistry|September 1, 1980
Evaluation of rotenone and related compounds as antagonists of slow-reacting substance of anaphylaxisR J Ashack, L P McCarty, R S Malek, et al.
Journal of Medical Genetics|November 5, 2002
Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13P Debeer, C Bacchelli, P J Scambler, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Clinical Genetics|April 3, 1999
Preaxial polydactyly in an infant with Down's syndromeA V Ramanan, K Hussain, S T Kempley, et al.
Clinical Genetics|March 22, 2001
Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLINC Bacchelli, F R Goodman, P J Scambler, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1993
How often should we measure the urinary anion gap for cases of suspected renal tubular acidosis?C P Streather, A O Phillips, F R Goodman, et al.
Circulation Research|November 1, 1972
Effects of added or substituted potassium ion on 45 Ca movements in rabbit aortic smooth muscleF R Goodman, G B Weiss, M N Weinberg, et al.
Prenatal Diagnosis|January 22, 2005
Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locusE K Bijlsma, A C Knegt, C M Bilardo, et al.
Journal of Cardiovascular Pharmacology|March 1, 1979
Effects of hypertonic mannitol on contractile responses and 45Ca movements in isolated canine arteriesF R Goodman, J T Willerson, R K Hester, et al.
Clinical and Experimental Hypertension. Part A, Theory and Practice|January 1, 1987
Central and peripheral inhibition of angiotensin converting enzyme (ACE) in the SHR: correlation with the antihypertensive activity of ACE inhibitorsJ A Norman, M Lehmann, F R Goodman, et al.
Clinical Genetics|August 16, 2003
ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndromeC Bacchelli, L C Wilson, J A Cook, et al.
Journal of Medicinal Chemistry|September 1, 1980
Evaluation of rotenone and related compounds as antagonists of slow-reacting substance of anaphylaxisR J Ashack, L P McCarty, R S Malek, et al.
Journal of Medical Genetics|November 5, 2002
Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13P Debeer, C Bacchelli, P J Scambler, et al.
Pageof 6