| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1986PNAS...83.5611W |
| P356 | DOI | 10.1073/PNAS.83.15.5611 |
| P932 | PMC publication ID | 386338 |
| P698 | PubMed publication ID | 3016709 |
| P5875 | ResearchGate publication ID | 20138990 |
| P2093 | author name string | C E Schwartz | |
| H F Willard | |||
| J S Waye | |||
| M H Skolnick | |||
| V E Powers | |||
| S B England | |||
| P2860 | cites work | Construction of a genetic linkage map in man using restriction fragment length polymorphisms | Q28263594 |
| The Formation, Structure, and Composition of the Mammalian Kinetochore and Kinetochore Fiber | Q34249698 | ||
| A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
| Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies | Q35570490 | ||
| Isolation and characterization of a major tandem repeat family from the human X chromosome | Q35673611 | ||
| Recent amplification of an alpha satellite DNA in humans | Q36134127 | ||
| Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome | Q36139991 | ||
| Characterization of a cloned repetitive DNA sequence concentrated on the human X chromosome | Q36318847 | ||
| Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment | Q36423793 | ||
| Chromosomal localization of complex and simple repeated human DNAs | Q36602964 | ||
| Linkage map of the short arm of human chromosome 11: location of the genes for catalase, calcitonin, and insulin-like growth factor II. | Q37525597 | ||
| Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variation | Q37561847 | ||
| Homology between human and simian repeated DNA | Q39646347 | ||
| A new era in mammalian gene mapping: somatic cell genetics and recombinant DNA methodologies | Q40126786 | ||
| The molecular structure of centromeres and telomeres | Q40186607 | ||
| The Wilhelmine E. Key 1979 Invitational Lecture: The anatomy of the human genome | Q40260159 | ||
| Sequence heterogeneity within the human alphoid repetitive DNA family | Q40560720 | ||
| Chromosome-specific organization of human alpha satellite DNA. | Q40611449 | ||
| Human chromosome heteromorphisms (variants). | Q43429248 | ||
| Construction of linkage maps with DNA markers for human chromosomes. | Q43486574 | ||
| DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man | Q45436146 | ||
| The genetic linkage map of the human X chromosome | Q45890080 | ||
| A cloned sequence, p82H, of the alphoid repeated DNA family found at the centromeres of all human chromosomes | Q48383646 | ||
| Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker. | Q55060411 | ||
| Localization of cystic fibrosis locus to human chromosome 7cen–q22 | Q57813752 | ||
| A closely linked genetic marker for cystic fibrosis | Q58278151 | ||
| A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 | Q59066375 | ||
| Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy | Q59080076 | ||
| Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome | Q60641517 | ||
| Long range periodicities in mouse satellite DNA | Q66946372 | ||
| Unequal crossover and the evolution of multigene families | Q69047999 | ||
| Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders | Q69805341 | ||
| Report of the Committee on Methods of Linkage Analysis and Reporting | Q69848402 | ||
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 5611-5615 | |
| P577 | publication date | 1986-08-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps | |
| P478 | volume | 83 |
| Q86614105 | A chromosome 5-specific repetitive DNA sequence in rice (Oryza sativa L) |
| Q41345422 | A genomic search for linkage of neurofibromatosis to RFLPs |
| Q35197967 | A human alpha satellite DNA subset specific for chromosome 12 |
| Q40524859 | A hypervariable RFLP within the ABR gene |
| Q69906467 | A hypervariable repeated sequence on human chromosome 1p36 |
| Q89425488 | Alpha satellite DNA biology: finding function in the recesses of the genome |
| Q70182723 | An improved method for detecting Y chromosomal DNA |
| Q51928487 | CENP-B box and pJalpha sequence distribution in human alpha satellite higher-order repeats (HOR). |
| Q64084268 | Centromere Repeats: Hidden Gems of the Genome |
| Q34063608 | Centromeres of human chromosomes |
| Q61998874 | Chapter 22 The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci |
| Q36695877 | Characterization of Murine Middle Repetitive DNA |
| Q35196488 | Characterization of a large deletion associated with a polymorphic block of repeated dinucleotides in the type III procollagen gene (COL3A1) of a patient with Ehlers-Danlos syndrome type IV. |
| Q69371516 | Chromosome specificity of satellite DNAs: short- and long-range organization of a diverged dimeric subset of human alpha satellite from chromosome 3 |
| Q35197471 | Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16 |
| Q69906461 | Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11 |
| Q68083338 | Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region |
| Q34481619 | Five polymorphic microsatellite VNTRs on the human X chromosome. |
| Q35247407 | Genetic analysis of eight loci tightly linked to neurofibromatosis 1 |
| Q35198265 | Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin |
| Q48237621 | Genome scanning by two-dimensional DNA typing: the use of repetitive DNA sequences for rapid mapping of genetic traits |
| Q40658233 | Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome |
| Q34718483 | Genomic organization of low copy number sequences that are associated with deca-satellite DNA in the monkey genome |
| Q35997271 | Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: implications for recombination between nonhomologues and Robertsonian translocations. |
| Q69834215 | Human satellite-III DNA: an example of a "macrosatellite" polymorphism |
| Q33965696 | Islands of complex DNA are widespread in Drosophila centric heterochromatin. |
| Q55060284 | Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes. |
| Q35247343 | Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type I. |
| Q69374429 | Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction |
| Q34323336 | Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability. |
| Q33828498 | Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified |
| Q40599169 | Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome. |
| Q41163434 | Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis |
| Q41590695 | Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line |
| Q35246214 | Molecular cytogenetic evidence for amplification of chromosome-specific alphoid sequences at enlarged C-bands on chromosome 6. |
| Q35247800 | Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome |
| Q33674852 | Molecular genetics of human chromosome 21. |
| Q58157413 | Molecular organization and chromosomal localization of six highly repeated DNA families in the bovine genome |
| Q41610185 | Molecular studies of parental origin and mosaicism in 45,X conceptuses |
| Q35247369 | Multipoint linkage analysis in neurofibromatosis type I: an international collaboration |
| Q24671930 | Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1 |
| Q38491324 | Non-random radial higher-order chromatin arrangements in nuclei of diploid human cells |
| Q36824341 | Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin |
| Q48351389 | Organization and evolution of alpha satellite DNA from human chromosome 11. |
| Q35935165 | PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA |
| Q35185266 | Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17. |
| Q67518843 | Reduced recombination and paternal age effect in Klinefelter syndrome |
| Q34373643 | Sequence analysis of a functional Drosophila centromere |
| Q68202233 | Structural organization and polymorphism of the alpha satellite DNA sequences of chromosomes 13 and 21 as revealed by pulse field gel electrophoresis |
| Q68292920 | TaqI reveals two independent alphoid polymorphisms on human chromosomes 13 and 21 |
| Q46067481 | The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17. |
| Q48069559 | The large-scale genomic organization of repetitive DNA families at the telomeres of rye chromosomes |
| Q35198614 | The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10 |
| Q35197998 | The parental origin of the extra X chromosome in 47,XXX females. |
| Q37665277 | The past, present, and future of human centromere genomics |
| Q35248326 | The probability of detecting the origin of nondisjunction of autosomal trisomies |
| Q35275936 | The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci |
| Q30501214 | The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus |
| Q24679370 | Uniparental disomy as a mechanism for human genetic disease |
Search more.