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J L Knight

Showing results (51-60 of 108) with videos related to

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American Journal of Hospital Pharmacy|November 1, 1976
Computer support of pharmaceutical services for ambulatory patientsA M Weissman, D K Solomon, R P Baumgartner, et al.
Clinical and Experimental Pharmacology & Physiology|September 19, 2001
Coronary artery baroreceptor-mediated changes in arterial pressure: a pilot study in conscious and anaesthetized sheepJ S Bennetts, L F Arnolda, H C Cullen, et al.
Clinical Case Reports|October 21, 2016
Activation of an exonic splice-donor site in exon 30 of <i>CDK5RAP2</i> in a patient with severe microcephaly and pigmentary abnormalitiesAlistair T Pagnamenta, Malcolm F Howard, Samantha J L Knight, et al.
Southern Medical Journal|May 1, 1970
Mass treatment for ascariasis: value of prophylactic use of piperazine in groups heavily infected with Ascaris lumbricoidesH S Pond, R B Bokat, J P Johnson, et al.
Psychiatric Genetics|June 5, 2003
Quantitation of X-Y homologous genes in patients with schizophrenia by multiplex polymerase chain reactionNorman L J Ross, Lampros A Mavrogiannis, Carole A Sargent, et al.
Genomic Medicine|October 17, 2008
Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United KingdomSarah Wordsworth, James Buchanan, Regina Regan, et al.
Anaesthesia and Intensive Care|October 16, 2007
Anticoagulation, bleeding and blood transfusion practices in Australasian cardiac surgical practiceD J Daly, P S Myles, J A Smith, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
The phenotype of Floating-Harbor syndrome in 10 patientsSusan M White, Angela Morgan, Annette Da Costa, et al.
Clinical Genetics|March 9, 2016
A de novo frameshift in HNRNPK causing a Kabuki-like syndrome with nodular heterotopiaL Lange, A T Pagnamenta, S Lise, et al.
European Journal of Human Genetics : EJHG|August 23, 2012
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorderDianne F Newbury, Francesca Mari, Elham Sadighi Akha, et al.
Pageof 11

Showing results (51-60 of 108) with videos related to

Sort By:
Pageof 11
American Journal of Hospital Pharmacy|November 1, 1976
Computer support of pharmaceutical services for ambulatory patientsA M Weissman, D K Solomon, R P Baumgartner, et al.
Clinical and Experimental Pharmacology & Physiology|September 19, 2001
Coronary artery baroreceptor-mediated changes in arterial pressure: a pilot study in conscious and anaesthetized sheepJ S Bennetts, L F Arnolda, H C Cullen, et al.
Clinical Case Reports|October 21, 2016
Activation of an exonic splice-donor site in exon 30 of <i>CDK5RAP2</i> in a patient with severe microcephaly and pigmentary abnormalitiesAlistair T Pagnamenta, Malcolm F Howard, Samantha J L Knight, et al.
Southern Medical Journal|May 1, 1970
Mass treatment for ascariasis: value of prophylactic use of piperazine in groups heavily infected with Ascaris lumbricoidesH S Pond, R B Bokat, J P Johnson, et al.
Psychiatric Genetics|June 5, 2003
Quantitation of X-Y homologous genes in patients with schizophrenia by multiplex polymerase chain reactionNorman L J Ross, Lampros A Mavrogiannis, Carole A Sargent, et al.
Genomic Medicine|October 17, 2008
Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United KingdomSarah Wordsworth, James Buchanan, Regina Regan, et al.
Anaesthesia and Intensive Care|October 16, 2007
Anticoagulation, bleeding and blood transfusion practices in Australasian cardiac surgical practiceD J Daly, P S Myles, J A Smith, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
The phenotype of Floating-Harbor syndrome in 10 patientsSusan M White, Angela Morgan, Annette Da Costa, et al.
Clinical Genetics|March 9, 2016
A de novo frameshift in HNRNPK causing a Kabuki-like syndrome with nodular heterotopiaL Lange, A T Pagnamenta, S Lise, et al.
European Journal of Human Genetics : EJHG|August 23, 2012
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorderDianne F Newbury, Francesca Mari, Elham Sadighi Akha, et al.
Pageof 11