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D Sillence

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

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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|June 10, 2000
Huntington's disease: neurological assessment of potential gene carriers presenting for predictive DNA testingE McCusker, F Richards, D Sillence, et al.
Bioscience Reports|December 10, 1999
Transport of (glyco)sphingolipids in and between cellular membranes; multidrug transporters and lateral domainsG van Meer, D Sillence, H Sprong, et al.
JIMD Reports|February 23, 2013
Combined Enzyme Replacement Therapy and Hematopoietic Stem Cell Transplantation in Mucopolysacharidosis Type VID Sillence, K Waters, S Donaldson, et al.
Archives of Disease in Childhood|August 1, 1993
Breathing abnormalities in sleep in achondroplasiaK A Waters, F Everett, D Sillence, et al.
Journal of Medical Genetics|September 11, 1998
Medical complications of achondroplasia: a multicentre patient reviewA G Hunter, A Bankier, J G Rogers, et al.
Pediatric Radiology|January 1, 1986
A new type of achondrogenesisK Kozlowski, T Tsuruta, N Taki, et al.
Pediatric Radiology|January 1, 1987
Perinatally lethal short rib-polydactyly syndromes. 1. Variability in known syndromesD Sillence, K Kozlowski, J Bar-ziv, et al.
Radiology|July 1, 1981
Diastrophic dysplasia: the death of a variantR Lachman, D Sillence, D Rimoin, et al.
Journal of Inherited Metabolic Disease|April 23, 2003
The osteodystrophy of mucolipidosis type III and the effects of intravenous pamidronate treatmentC Robinson, N Baker, J Noble, et al.
European Journal of Pediatrics|November 1, 1992
Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctataJ L Hughes, A Poulos, D I Crane, et al.
Pageof 6

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

Sort By:
Pageof 6
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|June 10, 2000
Huntington's disease: neurological assessment of potential gene carriers presenting for predictive DNA testingE McCusker, F Richards, D Sillence, et al.
Bioscience Reports|December 10, 1999
Transport of (glyco)sphingolipids in and between cellular membranes; multidrug transporters and lateral domainsG van Meer, D Sillence, H Sprong, et al.
JIMD Reports|February 23, 2013
Combined Enzyme Replacement Therapy and Hematopoietic Stem Cell Transplantation in Mucopolysacharidosis Type VID Sillence, K Waters, S Donaldson, et al.
Archives of Disease in Childhood|August 1, 1993
Breathing abnormalities in sleep in achondroplasiaK A Waters, F Everett, D Sillence, et al.
Journal of Medical Genetics|September 11, 1998
Medical complications of achondroplasia: a multicentre patient reviewA G Hunter, A Bankier, J G Rogers, et al.
Pediatric Radiology|January 1, 1986
A new type of achondrogenesisK Kozlowski, T Tsuruta, N Taki, et al.
Pediatric Radiology|January 1, 1987
Perinatally lethal short rib-polydactyly syndromes. 1. Variability in known syndromesD Sillence, K Kozlowski, J Bar-ziv, et al.
Radiology|July 1, 1981
Diastrophic dysplasia: the death of a variantR Lachman, D Sillence, D Rimoin, et al.
Journal of Inherited Metabolic Disease|April 23, 2003
The osteodystrophy of mucolipidosis type III and the effects of intravenous pamidronate treatmentC Robinson, N Baker, J Noble, et al.
European Journal of Pediatrics|November 1, 1992
Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctataJ L Hughes, A Poulos, D I Crane, et al.
Pageof 6