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Screening lambdagt recombinant clones by hybridization to single plaques in situ.
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Rat insulin genes: construction of plasmids containing the coding sequences.
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Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.
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Chromosomal anomalies in patients with retinoblastoma.
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Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.
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Induced segregation of human syntenic genes by 5-bromodeozyuridine + near-visible light.
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The isolation of structural genes from libraries of eucaryotic DNA.
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Cloning human fetal gamma globin and mouse alpha-type globin DNA: preparation and screening of shotgun collections.
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The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA.
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Regional assignment of human genes TPI1, GAPDH, LDHB, SHMT, and PEPB on chromosome 12.
Cytogenet Cell Genet. 1979;24(2):102-14
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Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate.
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RNA polymerase III transcriptional units are interspersed among human non-alpha-globin genes.
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Precise localization of human beta-globin gene complex on chromosome 11.
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Partial purification and characterization of DNA from the human X chromosome.
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Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
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Cloning and characterization of DNA sequences surrounding the human gamma-, delta-, and beta-globin genes.
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Nucleic acid spot hybridization: rapid quantitative screening of lymphoid cell lines for Epstein-Barr viral DNA.
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A family of long reiterated DNA sequences, one copy of which is next to the human beta globin gene.
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Chromosome abnormalities in human leukemia.
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A reliable method for the recovery of DNA fragments from agarose and acrylamide gels.
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Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry.
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The role of gene dosage and genetic transpositions in carcinogenesis.
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Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23).
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Isolation and chromosomal localization of unique DNA sequences from a human genomic library.
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The Alu family of dispersed repetitive sequences.
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Regional mapping of the gene coding for enolase-2 on human chromosome 12.
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