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

Por Pearson, P.L.
Publicado em 1991

The Chromosome. Structural and Functional Aspects

Por Pearson, P. L.
Publicado em 1968

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

Por Bobrow, M, Pearson, P L
Publicado em 1971

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

Por Beverstock, G C, Pearson, P L
Publicado em 1981

Sequence heterogeneity within the human alphoid repetitive DNA family.

Por Devilee, P, Slagboom, P, Cornelisse, C J, Pearson, P L
Publicado em 1986

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

Por Wapenaar, M.C., Pearson, P.L., Van Ommen, G.J.B.
Publicado em 1990

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

Por Veenema, H, Geraedts, J P, Beverstock, G C, Pearson, P L
Publicado em 1987

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

Por Scheffer, H, Penninga, D, Goor, N, Pearson, P L, Buys, C H
Publicado em 1986

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

Por Scheffer, H, Penninga, D, Goor, N, Pearson, P L, Buys, C H
Publicado em 1986

The GDB™ Human Genome Data Base Anno 1992

Por Pearson, P.L., Matheson, N.W., Flescher, D.C., Robbins, R.J.
Publicado em 1992

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

Por Kingston, H M, Thomas, N S, Pearson, P L, Sarfarazi, M, Harper, P S
Publicado em 1983

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

Por Dauwerse, H G, van Ommen, G B, Breuning, M H, Pearson, P L
Publicado em 1989

The GDB human genome data base anno 1993.

Por Cuticchia, A J, Fasman, K H, Kingsbury, D T, Robbins, R J, Pearson, P L
Publicado em 1993

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

Por Brown, C S, Pearson, P L, Thomas, N S, Sarfarazi, M, Harper, P S, Shaw, D J
Publicado em 1985

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

Por Hofker, M H, Breuning, M H, Bakker, E, van Ommen, G J, Pearson, P L
Publicado em 1985

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

Por Arveiler, B, Oberlé, I, Vincent, A, Hofker, M H, Pearson, P L, Mandel, J L
Publicado em 1988

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

Por Bakker, E, Skraastad, M I, Fisser-Groen, Y M, van Ommen, G J, Pearson, P L
Publicado em 1987

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

Por Breuning, M H, Dauwerse, J G, Saris, J J, van Ommen, G J, Pearson, P L
Publicado em 1989

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

Por Veenema, H, Carpenter, N J, Bakker, E, Hofker, M H, Ward, A M, Pearson, P L
Publicado em 1987

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

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