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.
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Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1Uniparental disomy as a mechanism for human genetic diseaseThe von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focusMolecular genetics of human chromosome 21.Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified.Islands of complex DNA are widespread in Drosophila centric heterochromatin.Centromeres of human chromosomes.Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability.Sequence analysis of a functional Drosophila centromereFive polymorphic microsatellite VNTRs on the human X chromosome.Genomic organization of low copy number sequences that are associated with deca-satellite DNA in the monkey genomePhysical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.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.Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16A human alpha satellite DNA subset specific for chromosome 12The parental origin of the extra X chromosome in 47,XXX females.Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of originThe mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10Molecular cytogenetic evidence for amplification of chromosome-specific alphoid sequences at enlarged C-bands on chromosome 6.Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type I.Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.Genetic analysis of eight loci tightly linked to neurofibromatosis 1Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.The probability of detecting the origin of nondisjunction of autosomal trisomiesPCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA.Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: implications for recombination between nonhomologues and Robertsonian translocations.Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin.The past, present, and future of human centromere genomics.A hypervariable RFLP within the ABR gene.Molecular analysis of a polymorphic domain of alpha satellite from the human X chromosome.Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome.A genomic search for linkage of neurofibromatosis to RFLPs.The large-scale genomic organization of repetitive DNA families at the telomeres of rye chromosomes.Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes.Molecular organization and chromosomal localization of six highly repeated DNA families in the bovine genome
P2860
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P2860
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.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
@tr
scientific article published on August 1986
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Detection of restriction fragm ...... re-based genetic linkage maps.
@en
Detection of restriction fragm ...... re-based genetic linkage maps.
@nl
type
label
Detection of restriction fragm ...... re-based genetic linkage maps.
@en
Detection of restriction fragm ...... re-based genetic linkage maps.
@nl
prefLabel
Detection of restriction fragm ...... re-based genetic linkage maps.
@en
Detection of restriction fragm ...... re-based genetic linkage maps.
@nl
P2093
P2860
P356
P1476
Detection of restriction fragm ...... re-based genetic linkage maps.
@en
P2093
C E Schwartz
H F Willard
M H Skolnick
S B England
V E Powers
P2860
P304
P356
10.1073/PNAS.83.15.5611
P407
P577
1986-08-01T00:00:00Z