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P H Dixon

Showing results (1-10 of 23) with videos related to

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Obstetric Medicine|September 2, 2016
The molecular genetics of intrahepatic cholestasis of pregnancyP H Dixon, C Williamson
American Journal of Human Genetics|January 23, 1999
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13S E Lloyd, A A Pannett, P H Dixon, et al.
American Journal of Human Genetics|July 27, 1999
Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3P F Worth, P Giunti, C Gardner-Thorpe, et al.
Placenta|May 21, 2011
Characterisation of the nuclear receptors FXR, PXR and CAR in normal and cholestatic placentaV L Geenes, P H Dixon, J Chambers, et al.
Journal of Medical Genetics|December 1, 1998
Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27D Trump, P H Dixon, S Mumm, et al.
American Journal of Human Genetics|March 20, 2001
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36E M Valente, A R Bentivoglio, P H Dixon, et al.
Brain : a Journal of Neurology|September 27, 2000
A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16E M Valente, S D Spacey, G M Wali, et al.
Placenta|November 23, 2013
Cholestatic pregnancy is associated with reduced placental 11βHSD2 expressionM Martineau, G Papacleovoulou, S Abu-Hayyeh, et al.
Clinical Endocrinology|January 7, 1999
GNAS1 mutational analysis in pseudohypoparathyroidismS F Ahmed, P H Dixon, D T Bonthron, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1997
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneityJ M Gertner, M P Whyte, P H Dixon, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Obstetric Medicine|September 2, 2016
The molecular genetics of intrahepatic cholestasis of pregnancyP H Dixon, C Williamson
American Journal of Human Genetics|January 23, 1999
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13S E Lloyd, A A Pannett, P H Dixon, et al.
American Journal of Human Genetics|July 27, 1999
Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3P F Worth, P Giunti, C Gardner-Thorpe, et al.
Placenta|May 21, 2011
Characterisation of the nuclear receptors FXR, PXR and CAR in normal and cholestatic placentaV L Geenes, P H Dixon, J Chambers, et al.
Journal of Medical Genetics|December 1, 1998
Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27D Trump, P H Dixon, S Mumm, et al.
American Journal of Human Genetics|March 20, 2001
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36E M Valente, A R Bentivoglio, P H Dixon, et al.
Brain : a Journal of Neurology|September 27, 2000
A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16E M Valente, S D Spacey, G M Wali, et al.
Placenta|November 23, 2013
Cholestatic pregnancy is associated with reduced placental 11βHSD2 expressionM Martineau, G Papacleovoulou, S Abu-Hayyeh, et al.
Clinical Endocrinology|January 7, 1999
GNAS1 mutational analysis in pseudohypoparathyroidismS F Ahmed, P H Dixon, D T Bonthron, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1997
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneityJ M Gertner, M P Whyte, P H Dixon, et al.
Pageof 3