Ngā hua rapu kaituhi

1

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

I whakaputaina 1999

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2

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

I whakaputaina 1980

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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3

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

I whakaputaina 1992

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4

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

I whakaputaina 1994

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5

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

I whakaputaina 1990

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6

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

I whakaputaina 1998

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7

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

I whakaputaina 1989

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8

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

I whakaputaina 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. mā Fain, P R, Wright, E, Willard, H F, Stephens, K, Barker, D F

I whakaputaina 1989

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10

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

I whakaputaina 1989

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11

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

I whakaputaina 1989

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12

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

I whakaputaina 1989

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13

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

I whakaputaina 1992

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14

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

I whakaputaina 1992

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15

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

I whakaputaina 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... mā 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

I whakaputaina 1989

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Ngā hua rapu - Barker, D F

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

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

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

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

Two polymorphisms of the FOS oncogene mā 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. mā Naumova, A K, Leppert, M, Barker, D F, Morgan, K, Sapienza, C

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

A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22). mā 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. mā Fain, P R, Wright, E, Willard, H F, Stephens, K, Barker, D F

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

MspI RFLP at CRYB1 locus (17q11.2----17q12). mā 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. mā 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. mā 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? mā 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. mā 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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