| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00286615 |
| P698 | PubMed publication ID | 6585346 |
| P2093 | author name string | H F Willard | |
| M T Holmes | |||
| P2860 | cites work | Differential expression of steroid sulphatase locus on active and inactive human X chromosome | Q24302242 |
| A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
| Evidence for X-linkage of steroid sulfatase in the mouse: steroid sulfatase levels in oocytes of XX and XO mice. | Q33949052 | ||
| Identification of an autosomal locus affecting steroid sulfatase activity among inbred strains of mice | Q33949499 | ||
| Regional assignment of the steroid sulfatase—X-linked ichthyosis locus: Implications for a noninactivated region on the short arm of human X chromosome | Q33981128 | ||
| Isolation and characterization of a major tandem repeat family from the human X chromosome | Q35673611 | ||
| Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts | Q36412160 | ||
| Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man. | Q36416283 | ||
| Non-inactivation of an X-Chromosome Locus in Man | Q39886266 | ||
| Clinical and biochemical investigations on patients with partial deficiency of placental steroid sulfatase | Q41448936 | ||
| Improved techniques for the induction of mammalian cell hybridization by polyethylene glycol | Q44952012 | ||
| Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes | Q45333368 | ||
| Cellulose acetate electrophoresis of human glucose-6-phosphate dehydrogenase. | Q53842251 | ||
| X-Linkage of Human α-Galactosidase | Q54593626 | ||
| Loss of human genetic markers in man--Chinese hamster somatic cell hybrids | Q71068742 | ||
| Regional assignment of the gene locus for steroid sulfatase | Q72123864 | ||
| Quantitative evaluation of electrophoretic allo- and isozyme patterns | Q72859069 | ||
| P433 | issue | 2-3 | |
| P304 | page(s) | 272-275 | |
| P577 | publication date | 1984-01-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids | |
| P478 | volume | 66 |
| Q34389945 | Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints |
| Q40611449 | Chromosome-specific organization of human alpha satellite DNA. |
| Q28287554 | Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism |
| Q68459268 | Gene for lipoamide dehydrogenase maps to human chromosome 7 |
| Q40658233 | Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome |
| Q41347455 | Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32. |
| Q24568191 | Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase |
| Q33259681 | Isolation, characterization and chromosomal localization of cDNA clones for the E1beta subunit of the pyruvate dehydrogenase complex |
| Q36885754 | Molecular cloning and chromosomal localization of DNA sequences associated with a human DNA repair gene |
| Q35197526 | Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect |
| Q69816528 | Organization and genomic distribution of "82H" alpha satellite DNA. Evidence for a low-copy or single-copy alphoid domain located on human chromosome 14 |
| Q36774465 | Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangement |
| Q41663873 | Physical mapping of 60 DNA markers in the p21.1 → q21.3 region of the human X chromosome |
| Q70101107 | Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19 |
| Q34379020 | The breakpoint of an inversion of chromosome 14 in a T-cell leukemia: sequences downstream of the immunoglobulin heavy chain locus are implicated in tumorigenesis |
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