The exon trapping assay partly discriminates against alternatively spliced exons.

od Andreadis, A, Nisson, P E, Kosik, K S, Watkins, P C
Izdano 1993

Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21.

od Antonarakis, S E, Kittur, S D, Metaxotou, C, Watkins, P C, Patel, A S
Izdano 1985

Molecular genetics of human chromosome 21.

od Watkins, P C, Tanzi, R E, Cheng, S V, Gusella, J F
Izdano 1987

A linkage study of cystic fibrosis in extended multigenerational pedigrees.

od Watkins, P C, Schwartz, R, Hoffman, N, Stanislovitis, P, Doherty, R, Klinger, K
Izdano 1986

Rapid detection of human chromosome 21 aberrations by in situ hybridization.

od Lichter, P, Cremer, T, Tang, C J, Watkins, P C, Manuelidis, L, Ward, D C
Izdano 1988

Three RFLPs are detected by an alpha spectrin genomic clone.

od Hoffman, N, Stanislovitis, P, Watkins, P C, Klinger, K W, Linnenbach, A J, Forget, B G
Izdano 1987

A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age.

od Tanzi, R E, Watkins, P C, Stewart, G D, Wexler, N S, Gusella, J F, Haines, J L
Izdano 1992

Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids.

od Van Keuren, M L, Watkins, P C, Drabkin, H A, Jabs, E W, Gusella, J F, Patterson, D
Izdano 1986

Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.

od Münke, M, Foellmer, B, Watkins, P C, Cowan, J M, Carroll, A J, Gusella, J F, Francke, U
Izdano 1988

Isolation of polymorphic DNA segments from human chromosome 21.

od Watkins, P C, Tanzi, R E, Gibbons, K T, Tricoli, J V, Landes, G, Eddy, R, Shows, T B, Gusella, J F
Izdano 1985

Genetic homogeneity of cystic fibrosis.

od Klinger, K, Stanislovitis, P, Hoffman, N, Watkins, P C, Schwartz, R, Doherty, R, Scambler, P, Farrall, M, Williamson, R, Wainwright, B
Izdano 1986

Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.

od Fujiwara, T M, Morgan, K, Schwartz, R H, Doherty, R A, Miller, S R, Klinger, K, Stanislovitis, P, Stuart, N, Watkins, P C
Izdano 1989

Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.

od Cheng, S V, Nadeau, J H, Tanzi, R E, Watkins, P C, Jagadesh, J, Taylor, B A, Haines, J L, Sacchi, N, Gusella, J F
Izdano 1988

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

od Rahmani, Z, Blouin, J L, Creau-Goldberg, N, Watkins, P C, Mattei, J F, Poissonnier, M, Prieur, M, Chettouh, Z, Nicole, A, Aurias, A
Izdano 1989

Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

od Phelan, M C, Morton, C C, Stevenson, R E, Tanzi, R E, Stewart, G D, Watkins, P C, Gusella, J F, Amos, J A
Izdano 1988

A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21.

od Kittur, S D, Antonarakis, S E, Tanzi, R E, Meyers, D A, Chakravarti, A, Groner, Y, Phillips, J A, Watkins, P C, Gusella, J F, Kazazian, H H
Izdano 1985