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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 CDK5RAP2 in a patient with severe microcephaly and pigmentary abnormalitiesAlistair T Pagnamenta, Malcolm F Howard, Samantha J L Knight, 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.
Cancers|December 5, 2019
Identification of Circulating Genomic and Metabolic Biomarkers in Intrahepatic CholangiocarcinomaHelen Winter, Pamela J Kaisaki, Joe Harvey, et al.
Pediatrics|July 21, 2010
Prevalence and complications of single-gene and chromosomal disorders in craniosynostosisAndrew O M Wilkie, Jo C Byren, Jane A Hurst, et al.
Human Molecular Genetics|April 10, 2015
Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposisAlistair T Pagnamenta, Malcolm F Howard, Eva Wisniewski, et al.
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