Pages that link to "Q36267955"
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The following pages link to Hurler's syndrome. A genetic study in cell culture (Q36267955):
Displaying 50 items.
- The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolism (Q28610244) (← links)
- The structure of acid mucopolysaccharides produced by Hurler fibroblasts in tissue culture (Q33562639) (← links)
- The mucopolysaccharidoses (Q33586932) (← links)
- Supravalvular aortic stenosis-infantile hypercalcaemia syndrome: in vitro hypersensitivity to vitamin D2 and calcium (Q33586970) (← links)
- A clinical and genetic study of Hunter's syndrome. 1. Heterogeneity (Q33669942) (← links)
- Progeria: a cell culture study on aging (Q34064382) (← links)
- Study of the Hurler syndrome using cell culture: definition of the biochemical phenotype and the effects of ascorbic acid on the mutant cell (Q34272120) (← links)
- Mucopolysaccharidoses and mucolipidoses (Q34302974) (← links)
- Synthesis and degradation of hyaluronic acid in the cultured fibroblasts of Marfan's disease (Q34510766) (← links)
- The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase (Q34719775) (← links)
- Simulation of genetic mucopolysaccharidoses in normal human fibroblasts by alteration of pH of the medium (Q34724220) (← links)
- Progress in birth defects research (Q34769279) (← links)
- Heritable disorders of mucopolysaccharide metabolism (Q34773597) (← links)
- The linkage relation of the loci for the Xm serum system and the X-linked form of Hurler's syndrome (Hunter's syndrome). (Q35231769) (← links)
- Genetics of protan and deutan color-vision anomalies: an instructive family (Q35231983) (← links)
- Cystic fibrosis: cell culture studies on a Danish population (Q35232487) (← links)
- Antenatal paediatrics by amniocentesis (Q36062511) (← links)
- Inhibition of cellular differentiation by phospholipase C. I. Effects of the enzyme on myogenesis and chondrogenesis in vitro (Q36195336) (← links)
- Hurler's syndrome. Effect of retinol (vitamin A alcohol) on cellular mucopolysaccharides in cultured human skin fibroblasts (Q36268654) (← links)
- Further studies on metachromasia in cultured human fibroblasts. Staining of glycosaminoglycans (mucopolysaccharides) by Alcian blue in salt solutions (Q36270473) (← links)
- Oyster ciliary inhibition by cystic fibrosis culture medium (Q36272143) (← links)
- Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture (Q36384007) (← links)
- Evidence for intergenic complementation in hybrid cells derived from two human diploid strains each carrying an X-linked mutation (Q36450660) (← links)
- Urinary excretion of glycosaminoglycans in the various forms of gargoylism (Q36540186) (← links)
- The genetic secrets of the humble fibroblast (Q36738484) (← links)
- Induced degradation of glycosaminoglycans in Hurler's and Hunter's syndromes by plasma infusion (Q37468016) (← links)
- Cytological and biochemical correlation of late X-chromosome replication and gene inactivation in the mule (Q37470743) (← links)
- Gene Expression in Cultured Mammalian Cells (Q39089352) (← links)
- Spectroscopic properties of complexes of acridine orange with glycosaminoglycans. I. Soluble complexes (Q39768372) (← links)
- Autoradiographic detection of mucopolysaccharide accumulation in single fibroblasts (Q39796072) (← links)
- Detection of inborn errors of metabolism (Q39885597) (← links)
- The Diagnosis of Mucopolysaccharidoses by Electron Microscopy of Skin Biopsies (Q39963073) (← links)
- Hurler's syndrome (Q40011083) (← links)
- Sulphated acid mucopolysaccharides in SV40-transformed human cells from normal and mucopolysaccharidosis patients (Q40088807) (← links)
- Prenatal diagnosis of inherited metabolic diseases; principles, pitfalls, and prospects. (Q40245324) (← links)
- Some studies on inherited disease using the techniques of cell culture (Q40340500) (← links)
- Antenatal diagnosis and treatment of the adrenogenital syndrome (Q43825663) (← links)
- Biochemical and ultrastructural studies in Hurler's syndrome (Q49124990) (← links)
- Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture (Q51122559) (← links)
- Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis (Q53691190) (← links)
- Chromosome analysis before birth and its value in genetic counselling. (Q53749365) (← links)
- The effect of retinol (vitamin-A alcohol) on urinary excretion of mucopolysaccharides in the Hurler syndrome. (Q53760383) (← links)
- Gaucher's Disease: A Genetic Disease Detected in Skin Fibroblast Cultures (Q53822815) (← links)
- Homocystinuria. (Q53883277) (← links)
- Diagnostic skin fibroblast culture. (Q53954337) (← links)
- A chemical method for the antenatal diagnosis of mucopolysaccharidoses. (Q54059446) (← links)
- Cell culture and rare connective tissue disorders. (Q54315351) (← links)
- Disinfection of lung ventilators. (Q54318792) (← links)
- Fucosidosis? (Q54442920) (← links)
- Serum-hexosaminidase levels in cystic fibrosis. (Q54470837) (← links)