Human chromosome-specific repetitive DNA probes: Targeting in situ hybridization to chromosome 17 with a 42-base-pair alphoid DNA oligomer
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference38 articles.
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2. Genomic organization of human centromeric alpha satellite DNA: Characterization of a chromosome 17 alpha satellite sequence;Choo;DNA,1987
3. Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: Diagnosis of trisomy 18 with probe L1.84;Cremer;Hum. Genet,1986
4. A comprehensive set of sequence analysis programs for the VAX;Devereux;Nucleic Acids Res,1984
5. Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21;Devilee;Cytogenet. Cell Genet,1986
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1. Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectively;Clinical Genetics;2008-06-28
2. Repetitive Elements;Wiley Encyclopedia of Molecular Medicine;2002-01-15
3. Overview of Human Repetitive DNA Sequences;Current Protocols in Human Genetics;2000-05
4. FISH analysis of the telomere sequences of bulldog ants (Myrmecia: Formicidae);Chromosoma;1995-10
5. Direction of DNA sequences within chromatids determined using strand-specific FISH;Chromosome Research;1995-09
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