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G T Besley

Showing results (41-50 of 69) with videos related to

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Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1984
Niemann-Pick disease type C with enhanced glycolipid storage. Report on further case of so-called lactosylceramidosisM Elleder, A Jirásek, F Smíd, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A case of the B1 variant of GM2-gangliosidosisR G Gray, A Green, L Rabb, et al.
Human Genetics|January 1, 1980
Somatic cell hybridisation studies showing different gene mutations in Niemann-Pick variantsG T Besley, A J Hoogeboom, A Hoogeveen, et al.
Lancet (London, England)|May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesisG T Besley, D M Broadhead, N C Nevin, et al.
Lancet (London, England)|December 16, 1978
Enzyme markers in acute lymphoblastic leukaemiaG T Besley, D M Broadhead, A D Bain, et al.
Prenatal Diagnosis|July 1, 1988
First trimester diagnosis of Gaucher disease in a fetus with trisomy 21G T Besley, M E Ferguson-Smith, C Frew, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndromeP T Clayton, D C Kalter, D J Atherton, et al.
British Journal of Haematology|January 1, 1985
Lysosomal isoenzyme profiles used to classify a case of acute undifferentiated leukaemiaO B Eden, P Darbyshire, R M Simpson, et al.
The Journal of Investigative Dermatology|December 1, 1990
Depletion of alcohol (hexanol) dehydrogenase activity in the epidermis and jejunal mucosa in Sjögren-Larsson syndromeM R Judge, B D Lake, V V Smith, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Mitochondrial complex deficiencies in a male with cardiomyopathy and 3-methylglutaconic aciduriaG T Besley, M Lendon, D M Broadhead, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1984
Niemann-Pick disease type C with enhanced glycolipid storage. Report on further case of so-called lactosylceramidosisM Elleder, A Jirásek, F Smíd, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A case of the B1 variant of GM2-gangliosidosisR G Gray, A Green, L Rabb, et al.
Human Genetics|January 1, 1980
Somatic cell hybridisation studies showing different gene mutations in Niemann-Pick variantsG T Besley, A J Hoogeboom, A Hoogeveen, et al.
Lancet (London, England)|May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesisG T Besley, D M Broadhead, N C Nevin, et al.
Lancet (London, England)|December 16, 1978
Enzyme markers in acute lymphoblastic leukaemiaG T Besley, D M Broadhead, A D Bain, et al.
Prenatal Diagnosis|July 1, 1988
First trimester diagnosis of Gaucher disease in a fetus with trisomy 21G T Besley, M E Ferguson-Smith, C Frew, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndromeP T Clayton, D C Kalter, D J Atherton, et al.
British Journal of Haematology|January 1, 1985
Lysosomal isoenzyme profiles used to classify a case of acute undifferentiated leukaemiaO B Eden, P Darbyshire, R M Simpson, et al.
The Journal of Investigative Dermatology|December 1, 1990
Depletion of alcohol (hexanol) dehydrogenase activity in the epidermis and jejunal mucosa in Sjögren-Larsson syndromeM R Judge, B D Lake, V V Smith, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Mitochondrial complex deficiencies in a male with cardiomyopathy and 3-methylglutaconic aciduriaG T Besley, M Lendon, D M Broadhead, et al.
Pageof 7