The genome data base (GDB)—a human gene mapping repository

gan Pearson, P.L.
Cyhoeddwyd 1991

The Chromosome. Structural and Functional Aspects

gan Pearson, P. L.
Cyhoeddwyd 1968

The use of quinacrine fluorescence in the identification of B and E group chromosomes involved in structural abnormalities.

gan Bobrow, M, Pearson, P L
Cyhoeddwyd 1971

Membrane fluidity measurements in peripheral cells from Huntington's disease patients

gan Beverstock, G C, Pearson, P L
Cyhoeddwyd 1981

Sequence heterogeneity within the human alphoid repetitive DNA family.

gan Devilee, P, Slagboom, P, Cornelisse, C J, Pearson, P L
Cyhoeddwyd 1986

P9 (DXYS75) detects a VNTR-type RFLP in the pseudoautosomal region

gan Wapenaar, M.C., Pearson, P.L., Van Ommen, G.J.B.
Cyhoeddwyd 1990

The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations.

gan Veenema, H, Geraedts, J P, Beverstock, G C, Pearson, P L
Cyhoeddwyd 1987

An anonymous single copy genomic clone at 13q12-13q13 identifies three RFLPs [HGM8 assignment no. D13S11].

gan Scheffer, H, Penninga, D, Goor, N, Pearson, P L, Buys, C H
Cyhoeddwyd 1986

A four-allele RFLP identified by an anonymous single copy genomic clone at 13q21-13qter [HGM8 assignment no. D13S12]

gan Scheffer, H, Penninga, D, Goor, N, Pearson, P L, Buys, C H
Cyhoeddwyd 1986

The GDB™ Human Genome Data Base Anno 1992

gan Pearson, P.L., Matheson, N.W., Flescher, D.C., Robbins, R.J.
Cyhoeddwyd 1992

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.

gan Kingston, H M, Thomas, N S, Pearson, P L, Sarfarazi, M, Harper, P S
Cyhoeddwyd 1983

Cosmid vector pCpG and plasmid vector pKNUN1, and their use for cloning DNA sequences adjacent to sites for rare cutting restriction endonucleases.

gan Dauwerse, H G, van Ommen, G B, Breuning, M H, Pearson, P L
Cyhoeddwyd 1989

The GDB human genome data base anno 1993.

gan Cuticchia, A J, Fasman, K H, Kingsbury, D T, Robbins, R J, Pearson, P L
Cyhoeddwyd 1993

Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.

gan Brown, C S, Pearson, P L, Thomas, N S, Sarfarazi, M, Harper, P S, Shaw, D J
Cyhoeddwyd 1985

An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI.

gan Hofker, M H, Breuning, M H, Bakker, E, van Ommen, G J, Pearson, P L
Cyhoeddwyd 1985

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.

gan Arveiler, B, Oberlé, I, Vincent, A, Hofker, M H, Pearson, P L, Mandel, J L
Cyhoeddwyd 1988

Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studies.

gan Bakker, E, Skraastad, M I, Fisser-Groen, Y M, van Ommen, G J, Pearson, P L
Cyhoeddwyd 1987

RFLP for an anonymous single copy clone at 16pter-16p13.1 [D16S127]

gan Breuning, M H, Dauwerse, J G, Saris, J J, van Ommen, G J, Pearson, P L
Cyhoeddwyd 1989

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

gan Veenema, H, Carpenter, N J, Bakker, E, Hofker, M H, Ward, A M, Pearson, P L
Cyhoeddwyd 1987

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.

gan Davies, K E, Pearson, P L, Harper, P S, Murray, J M, O'Brien, T, Sarfarazi, M, Williamson, R
Cyhoeddwyd 1983