Resultats de la cerca - Barker, D F

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

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

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

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

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Two polymorphisms of the FOS oncogene per 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. per 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). per 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). per 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. per 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). per 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). per 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. per 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. per 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? per 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. per 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... per 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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