| P50 | author | James F. Gusella | Q1602688 |
| | Xandra O. Breakefield | Q63607934 |
| P2093 | author name string | Fahn S | |
| | Kramer PL | |
| | Kidd KK | |
| | Ozelius L | |
| P2860 | cites work | Strategies for multilocus linkage analysis in humans | Q27860521 |
| | Chromosomal localization of human β globin gene on human chromosome 11 in somatic cell hybrids | Q33968747 |
| | A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 |
| | Isolation and preliminary characterization of a human transforming gene from T24 bladder carcinoma cells | Q34277765 |
| | Isolation of polymorphic DNA segments from human chromosome 21. | Q35559585 |
| | Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction | Q36144282 |
| | DNA polymorphism and molecular pathology of the human globin gene clusters | Q39813814 |
| | The torsion dystonias: Literature review and genetic and clinical studies | Q40060317 |
| | A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7. | Q41998207 |
| | The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus. | Q52078575 |
| | Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms | Q70144573 |
| | Chromosome 13 restriction fragment length polymorphisms | Q70184689 |
| | Studies on dystonia musculorum deformans | Q79538561 |
| P433 | issue | 5 | |
| P304 | page(s) | 377-386 | |
| P577 | publication date | 1987-01-01 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis | |
| P478 | volume | 4 | |