Search research articles
Contact Us
Filters
Showing results (31-40 of 52) with videos related to
Page
of 6
Sort By:
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 testing
E 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 domains
G 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 VI
D Sillence, K Waters, S Donaldson, et al.
Archives of Disease in Childhood
|
August 1, 1993
Breathing abnormalities in sleep in achondroplasia
K A Waters, F Everett, D Sillence, et al.
Journal of Medical Genetics
|
September 11, 1998
Medical complications of achondroplasia: a multicentre patient review
A G Hunter, A Bankier, J G Rogers, et al.
Pediatric Radiology
|
January 1, 1986
A new type of achondrogenesis
K Kozlowski, T Tsuruta, N Taki, et al.
Pediatric Radiology
|
January 1, 1987
Perinatally lethal short rib-polydactyly syndromes. 1. Variability in known syndromes
D Sillence, K Kozlowski, J Bar-ziv, et al.
Radiology
|
July 1, 1981
Diastrophic dysplasia: the death of a variant
R 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 treatment
C Robinson, N Baker, J Noble, et al.
European Journal of Pediatrics
|
November 1, 1992
Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctata
J L Hughes, A Poulos, D I Crane, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 52) with videos related to
Sort By:
Page
of 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 testing
E 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 domains
G 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 VI
D Sillence, K Waters, S Donaldson, et al.
Archives of Disease in Childhood
|
August 1, 1993
Breathing abnormalities in sleep in achondroplasia
K A Waters, F Everett, D Sillence, et al.
Journal of Medical Genetics
|
September 11, 1998
Medical complications of achondroplasia: a multicentre patient review
A G Hunter, A Bankier, J G Rogers, et al.
Pediatric Radiology
|
January 1, 1986
A new type of achondrogenesis
K Kozlowski, T Tsuruta, N Taki, et al.
Pediatric Radiology
|
January 1, 1987
Perinatally lethal short rib-polydactyly syndromes. 1. Variability in known syndromes
D Sillence, K Kozlowski, J Bar-ziv, et al.
Radiology
|
July 1, 1981
Diastrophic dysplasia: the death of a variant
R 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 treatment
C Robinson, N Baker, J Noble, et al.
European Journal of Pediatrics
|
November 1, 1992
Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctata
J L Hughes, A Poulos, D I Crane, et al.
Page
of 6