Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.

Por Liu, X, Barker, D F
Publicado em 1999

Use of bio-lac fusion strains to study regulation of biotin biosynthesis in Escherichia coli.

Por Barker, D F, Campbell, A M
Publicado em 1980

Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22

Por Barker, D.F., Cleverly, J., Fain, P.R.
Publicado em 1992

Two polymorphisms of the FOS oncogene

Por Siewertsen, M.A., Barker, D.F., Cox, D.W.
Publicado em 1990

Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy.

Por Fain, P. R., Barker, D. F., Chance, P. F.
Publicado em 1994

Two polymorphic TaqI sites at the human NGFR locus (17q12----17q22).

Por Wright, E C, Fain, P R, Barker, D F, Chao, M V
Publicado em 1989

A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22).

Por Wright, E C, Fain, P R, Barker, D F, Chao, M V
Publicado em 1989

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

Por Naumova, A K, Leppert, M, Barker, D F, Morgan, K, Sapienza, C
Publicado em 1998

The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints.

Por Fain, P R, Wright, E, Willard, H F, Stephens, K, Barker, D F
Publicado em 1989

A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12).

Por Barker, D F, Fain, P R, Wright, E C, Nguyen, K, Tsui, L C
Publicado em 1989

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

Por Barker, D F, Fain, P R, Wright, E C, Nguyen, K, Tsui, L C
Publicado em 1989

Refined physical and genetic mapping of the NF1 region on chromosome 17.

Por Fain, P R, Goldgar, D E, Wallace, M R, Collins, F S, Wright, E, Nguyen, K, Barker, D F
Publicado em 1989

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers.

Por Lebo, R V, Lynch, E D, Bird, T D, Golbus, M S, Barker, D F, O'Connell, P, Chance, P F
Publicado em 1992

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

Por Stern, H J, Saal, H M, Lee, J S, Fain, P R, Goldgar, D E, Rosenbaum, K N, Barker, D F
Publicado em 1992

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

Por Barker, D. F., Pruchno, C. J., Jiang, X., Atkin, C. L., Stone, E. M., Denison, J. C., Fain, P. R., Gregory, M. C.
Publicado em 1996

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

Por 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
Publicado em 1989