The deficiency of a lysosomal acid hydrolase in two clones derived from the human lymphoblastoid line F137 after mutagen treatment
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1977.tb01958.x/fullpdf
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4. Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes.
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1. Sialidosis Type 1;Annals of Human Genetics;2007-09-28
2. Expression of human transferrin receptor is controlled by a gene on chromosome 3: Assignment using species specificity of a monoclonal antibody;Somatic Cell Genetics;1982-03
3. Deficiency of malic enzyme: a possible marker for malignancy in lymphoid cells;Annals of Human Genetics;1981-07
4. Differences in genetic stability between human cell lines from patients with and without lymphoreticular malignancy;Annals of Human Genetics;1980-10
5. Lysosomal enzymes in human lymphoblastoid lines: unusual characteristics of RAJI and DAUDI;Annals of Human Genetics;1977-07
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