P. O'Connell

The CEPH consortium linkage map of human chromosome 1.

R L White, K H Buetow, J M Lalouel, 1991, Genomics.

Isolation and mapping of a polymorphic DNA sequence (pTHH59) on chromosome 17q [D17S4].

Y. Nakamura, M. Leppert, P. O'Connell, 1988, Nucleic acids research.

Isolation and mapping of a polymorphic DNA sequence (pMCOA12) on chromosome 9q [D9S28].

Y. Nakamura, G. Lathrop, L. Ballard, 1988, Nucleic acids research.

Etiological heterogeneity in X-linked spastic paraplegia.

Y. Nakamura, M. Leppert, P. O'Connell, 1987, American journal of human genetics.

cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene.

P. O'Connell, M. Culver, R. Cawthon, 1991, Genomics.

Twelve loci form a continuous linkage map for human chromosome 18.

Y. Nakamura, M. Leppert, P. O'Connell, 1988, Genomics.

A breast-ovarian cancer susceptibility gene maps to chromosome 17q21.

P. O'Connell, R. White, G. Lenoir, 1993, American journal of human genetics.