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Large scale cDNA sequencing for analysis of quantitative and qualitative aspects of gene expressionpp173 - 179 Kousaku Okubo, Naohiro Hori, Ryo Matoba, Toshiyuki Niiyama, Atsushi Fukushima, Yuko Kojima
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Single pass sequencing and physical and genetic mapping of human brain cDNAspp180 - 185 Akbar S. Khan, Andrea S. Wilcox, Mihael H. Polymeropoulos, Janet A. Hopkins, Tamara J. Stevens, Misi Robinson, Arto K. Orpana
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Human genes containing polymorphic trinucleotide repeatspp186 - 191 Gregory J. Riggins, Laurie K. Lokey, Jane L. Chastain, Harold A. Leiner, Stephanie L. Sherman, Keith D. Wilkinson
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X inactivation in mammalian testis is correlated with inactive X−specific transcriptionpp192 - 195 Carmelit Richler, Hermona Soreq
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Expression of the X−inactivation−associated gene XIST during spermatogenesispp196 - 199 Eduardo C. Salido, Pauline H. Yen, Thuluvancheri K. Mohandas
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Expression of Xist in mouse germ cells correlates with X−chromosome inactivationpp200 - 203 John R. McCarrey
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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finlandpp204 - 211 Johanna Hästbacka, Albert de la Chapelle, Ilkka Kaitila, Pertti Sistonen, Alix Weaver
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Cloning of the −adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplificationpp223 - 227 S.A.M. Taylor, R.G. Snell, A. Buckler, C. Ambrose, M. Duyao, D. Church, C.S. Lin, M. Altherr, G.P. Bates, N. Groot, G. Barnes, D.J. Shaw, H. Lehrach, J.J. Wasmuth, P.S. Harper, D.E. Housman, M.E. MacDonald
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A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers−Danlos syndrome type VIpp228 - 231 James Hyland, Leena Ala-Kokko, Peter Royce, Beat Steinmann, Kari I. Kivirikko
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Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 genepp232 - 239 Tom Glaser, David S. Walton
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Submucosal glands are the predominant site of CFTR expression in the human bronchuspp240 - 248 John F. Engelhardt, James R. Yankaskas, Stephen A. Ernst, Yiping Yang, Christopher R. Marino, Richard C. Boucher, Jonathan A. Cohn
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−adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification
