Search research articles
Contact Us
Filters
Showing results (41-50 of 69) with videos related to
Page
of 7
Sort By:
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 lactosylceramidosis
M Elleder, A Jirásek, F Smíd, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
A case of the B1 variant of GM2-gangliosidosis
R G Gray, A Green, L Rabb, et al.
Human Genetics
|
January 1, 1980
Somatic cell hybridisation studies showing different gene mutations in Niemann-Pick variants
G T Besley, A J Hoogeboom, A Hoogeveen, et al.
Lancet (London, England)
|
May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesis
G T Besley, D M Broadhead, N C Nevin, et al.
Lancet (London, England)
|
December 16, 1978
Enzyme markers in acute lymphoblastic leukaemia
G 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 21
G 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 syndrome
P 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 leukaemia
O 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 syndrome
M 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 aciduria
G T Besley, M Lendon, D M Broadhead, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 69) with videos related to
Sort By:
Page
of 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 lactosylceramidosis
M Elleder, A Jirásek, F Smíd, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
A case of the B1 variant of GM2-gangliosidosis
R G Gray, A Green, L Rabb, et al.
Human Genetics
|
January 1, 1980
Somatic cell hybridisation studies showing different gene mutations in Niemann-Pick variants
G T Besley, A J Hoogeboom, A Hoogeveen, et al.
Lancet (London, England)
|
May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesis
G T Besley, D M Broadhead, N C Nevin, et al.
Lancet (London, England)
|
December 16, 1978
Enzyme markers in acute lymphoblastic leukaemia
G 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 21
G 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 syndrome
P 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 leukaemia
O 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 syndrome
M 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 aciduria
G T Besley, M Lendon, D M Broadhead, et al.
Page
of 7