Torthaí cuardaigh - Barker, D F

Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1. de réir Liu, X, Barker, D F

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Use of bio-lac fusion strains to study regulation of biotin biosynthesis in Escherichia coli. de réir Barker, D F, Campbell, A M

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Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22 de réir Barker, D.F., Cleverly, J., Fain, P.R.

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Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy. de réir Fain, P. R., Barker, D. F., Chance, P. F.

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Two polymorphisms of the FOS oncogene de réir Siewertsen, M.A., Barker, D.F., Cox, D.W.

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Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. de réir Naumova, A K, Leppert, M, Barker, D F, Morgan, K, Sapienza, C

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Two polymorphic TaqI sites at the human NGFR locus (17q12----17q22). de réir Wright, E C, Fain, P R, Barker, D F, Chao, M V

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A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22). de réir Wright, E C, Fain, P R, Barker, D F, Chao, M V

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The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints. de réir Fain, P R, Wright, E, Willard, H F, Stephens, K, Barker, D F

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A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12). de réir Barker, D F, Fain, P R, Wright, E C, Nguyen, K, Tsui, L C

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MspI RFLP at CRYB1 locus (17q11.2----17q12). de réir Barker, D F, Fain, P R, Wright, E C, Nguyen, K, Tsui, L C

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Refined physical and genetic mapping of the NF1 region on chromosome 17. de réir Fain, P R, Goldgar, D E, Wallace, M R, Collins, F S, Wright, E, Nguyen, K, Barker, D F

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Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers. de réir Lebo, R V, Lynch, E D, Bird, T D, Golbus, M S, Barker, D F, O'Connell, P, Chance, P F

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Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? de réir Stern, H J, Saal, H M, Lee, J S, Fain, P R, Goldgar, D E, Rosenbaum, K N, Barker, D F

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A mutation causing Alport syndrome with tardive hearing loss is common in the western United States. de réir Barker, D. F., Pruchno, C. J., Jiang, X., Atkin, C. L., Stone, E. M., Denison, J. C., Fain, P. R., Gregory, M. C.

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Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromo... de réir Ledbetter, D H, Ledbetter, S A, vanTuinen, P, Summers, K M, Robinson, T J, Nakamura, Y, Wolff, R, White, R, Barker, D F, Wallace, M R

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