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Hum Genet. 1987; 76(2):191-5.
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Studies of a DNA marker (G8) genetically linked to Huntington disease in British families.
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Hum Genet. 1986; 73(4):333-9.
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Human J chain gene: chromosomal localization and associated restriction fragment length polymorphisms.
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Proc Natl Acad Sci U S A. 1986; 83(15):5592-6.
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Molecular genetics of human chromosome 4.
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Regional localization of chromosome 3-specific DNA fragments by using a hybrid cell deletion mapping panel.
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Am J Hum Genet. 1988; 43(4):442-51.
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Pairwise linkage analysis of 11 loci on human chromosome 4.
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Am J Hum Genet. 1988; 42(3):490-7.
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Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma.
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Proc Natl Acad Sci U S A. 1988; 85(5):1571-5.
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Isolation and mapping of a polymorphic DNA sequence pYNZ86.1 on chromosome 3 (D3S30).
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Nucleic Acids Res. 1987; 15(23):10079.
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Isolation of polymorphic DNA fragments from human chromosome 4.
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Nucleic Acids Res. 1987; 15(4):1445-58.
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Mapping studies of the serum cholinesterase-2 locus (CHE2).
Marazita M, Keats B, Spence M, Sparkes R, Field L, Sparkes M
Hum Genet. 1989; 83(2):139-44.
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Identification of two cosmids derived from within chromosomal band 3p21.1 that contain clusters of rare restriction sites and evolutionarily conserved sequences.
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Am J Hum Genet. 1989; 45(3):443-7.
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Lack of expression of aminoacylase-1 in small cell lung cancer. Evidence for inactivation of genes encoded by chromosome 3p.
Miller Y, Minna J, Gazdar A
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