Rezultati pretrage autora

1

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

Izdano 1999

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2

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

Izdano 1980

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3

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

Izdano 1992

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4

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

Izdano 1994

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5

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

Izdano 1990

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6

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

Izdano 1998

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7

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

Izdano 1989

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8

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

Izdano 1989

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9

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

Izdano 1989

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10

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

Izdano 1989

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11

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

Izdano 1989

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12

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

Izdano 1989

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13

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

Izdano 1992

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14

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

Izdano 1992

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15

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

Izdano 1996

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16

Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromo... od 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

Izdano 1989

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Rezultati pretrage - Barker, D F

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

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

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

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

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

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

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

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

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

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

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

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

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

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

A mutation causing Alport syndrome with tardive hearing loss is common in the western United States. od 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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