| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1990PNAS...87.5754K |
| P356 | DOI | 10.1073/PNAS.87.15.5754 |
| P932 | PMC publication ID | 54406 |
| P698 | PubMed publication ID | 2377614 |
| P5875 | ResearchGate publication ID | 20777705 |
| P2093 | author name string | Falls K | |
| Green P | |||
| Hogan C | |||
| Reeders ST | |||
| Brown VA | |||
| Keith TP | |||
| Powers JA | |||
| Phipps P | |||
| Bricker A | |||
| Rediker KS | |||
| P2860 | cites work | Molecular basis of length polymorphism in the human zeta-globin gene complex | Q24594782 |
| A highly polymorphic locus in human DNA | Q24608722 | ||
| Construction of a genetic linkage map in man using restriction fragment length polymorphisms | Q28263594 | ||
| The structure of the human zeta-globin gene and a closely linked, nearly identical pseudogene | Q28265105 | ||
| Polymorphic DNA region adjacent to the 5' end of the human insulin gene | Q29618325 | ||
| Genetic linkage in the horse. II. Distribution of male recombination estimates and the influence of age, breed and sex on recombination frequency. | Q33949798 | ||
| Localization of the human haptoglobin genes distal to the fragile site at 16q22 using in situ hybridization | Q34179651 | ||
| Construction of multilocus genetic linkage maps in humans | Q34180045 | ||
| Duplication within the haptoglobin Hp2 gene | Q34255663 | ||
| Genetic linkage map of human chromosome 7 with 63 DNA markers | Q34365588 | ||
| Identification of more than 500 RFLPs by screening random genomic clones | Q35246565 | ||
| New approach for isolation of VNTR markers. | Q35248153 | ||
| A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library | Q36414869 | ||
| A highly polymorphic locus in human DNA revealed by cosmid-derived probes | Q36423825 | ||
| Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster | Q36425658 | ||
| Cloning of a functional human adenine phosphoribosyltransferase (APRT) gene: Identification of a restriction fragment length polymorphism and preliminary analysis of DNAs from APRT-deficient families and cell mutants | Q36586672 | ||
| Double cos site vectors: simplified cosmid cloning. | Q36598612 | ||
| Data and theory for a revised chiasma map of man. | Q36651497 | ||
| Strategies for studying heterogeneous genetic traits in humans by using a linkage map of restriction fragment length polymorphisms | Q37401497 | ||
| Diagnosis of genetic disorders at the DNA level | Q38597743 | ||
| A new hypervariable marker for the human alpha-globin gene cluster | Q41990215 | ||
| A primary map of 24 loci on human chromosome 16. | Q43438436 | ||
| Construction of linkage maps with DNA markers for human chromosomes. | Q43486574 | ||
| A primary genetic linkage map for human chromosome 12. | Q43577770 | ||
| Simultaneous genetic mapping of multiple human minisatellite sequences using DNA fingerprinting | Q43771470 | ||
| A mapped set of DNA markers for human chromosome 15. | Q44747553 | ||
| The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions | Q47617863 | ||
| A mapped set of DNA markers for human chromosome 17. | Q52566492 | ||
| A genetic linkage map of the human genome. | Q52586464 | ||
| A mouse-human hybrid cell panel for mapping human chromosome 16. | Q52829176 | ||
| A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 | Q59066375 | ||
| A new location for the human adenine phosphoribosyltransferase gene ( APRT ) distal to the haptoglobin ( HP ) and fra(16)(q23) ( FRAUD ) loci | Q63681886 | ||
| Clustering of hypervariable minisatellites in the proterminal regions of human autosomes | Q68062252 | ||
| A genetic linkage map of 32 loci on human chromosome 10 | Q69376849 | ||
| A genetic linkage map of markers for human chromosome 20 | Q69394270 | ||
| Unusual recombination values and the mapping of the lethal miniature in the house mouse | Q69447671 | ||
| A primary map of ten DNA markers and two serological markers for human chromosome 19 | Q69929783 | ||
| Regional localization of the autosomal dominant polycystic kidney disease locus | Q69930150 | ||
| Human alpha-globin maps to pter-p13.3 in chromosome 16 distal to PGP | Q70182727 | ||
| Sex differences in recombination of linked genes in animals | Q72264586 | ||
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 5754-5758 | |
| P577 | publication date | 1990-08-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Genetic linkage map of 46 DNA markers on human chromosome 16. | |
| P478 | volume | 87 |
| Q58803778 | A population genomic characterization of copy number variation in the opportunistic fungal pathogen Aspergillus fumigatus |
| Q52284214 | Alternative test for linkage between two loci. |
| Q35194066 | Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysis |
| Q35364327 | Comparative map for mice and humans |
| Q67871559 | Comparative map for mice and humans |
| Q33667362 | Extensive Copy Number Variation in Fermentation-Related Genes Among Saccharomyces cerevisiae Wine Strains |
| Q67518183 | Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD |
| Q35194242 | Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16 |
| Q79280583 | Molecular mapping of four ovule lethal mutants in soybean |
| Q35194870 | Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies |
| Q24670091 | Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12 |
| Q35194477 | Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3. |
| Q35889300 | Somatic mosaicism for a newly identified splice-site mutation in a patient with adenosine deaminase-deficient immunodeficiency and spontaneous clinical recovery |
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