Jenkins T - Search Results

1

Genetic and physical mapping and population studies of a fibronectin receptor beta-subunit-like sequence on human chromosome 19.

Giuffra LA, Lichter P, Wu JS, Kennedy JL, Pakstis AJ, Rogers J, Kidd JR, Harley H, Jenkins T, Ward DC, et al. Giuffra LA, et al. Among authors: jenkins t. Genomics. 1990 Oct;8(2):340-6. doi: 10.1016/0888-7543(90)90291-2. Genomics. 1990. PMID: 1979054

2

A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus.

Kidd KK, Morar B, Castiglione CM, Zhao H, Pakstis AJ, Speed WC, Bonne-Tamir B, Lu RB, Goldman D, Lee C, Nam YS, Grandy DK, Jenkins T, Kidd JR. Kidd KK, et al. Among authors: jenkins t. Hum Genet. 1998 Aug;103(2):211-27. doi: 10.1007/s004390050809. Hum Genet. 1998. PMID: 9760208

3

A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.

Tishkoff SA, Goldman A, Calafell F, Speed WC, Deinard AS, Bonne-Tamir B, Kidd JR, Pakstis AJ, Jenkins T, Kidd KK. Tishkoff SA, et al. Among authors: jenkins t. Am J Hum Genet. 1998 Jun;62(6):1389-402. doi: 10.1086/301861. Am J Hum Genet. 1998. PMID: 9585589 Free PMC article.

4

Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.

Tishkoff SA, Pakstis AJ, Stoneking M, Kidd JR, Destro-Bisol G, Sanjantila A, Lu RB, Deinard AS, Sirugo G, Jenkins T, Kidd KK, Clark AG. Tishkoff SA, et al. Among authors: jenkins t. Am J Hum Genet. 2000 Oct;67(4):901-25. doi: 10.1086/303068. Epub 2000 Sep 13. Am J Hum Genet. 2000. PMID: 10986042 Free PMC article.

5

Y chromosome sequence variation and the history of human populations.

Underhill PA, Shen P, Lin AA, Jin L, Passarino G, Yang WH, Kauffman E, Bonné-Tamir B, Bertranpetit J, Francalacci P, Ibrahim M, Jenkins T, Kidd JR, Mehdi SQ, Seielstad MT, Wells RS, Piazza A, Davis RW, Feldman MW, Cavalli-Sforza LL, Oefner PJ. Underhill PA, et al. Among authors: jenkins t. Nat Genet. 2000 Nov;26(3):358-61. doi: 10.1038/81685. Nat Genet. 2000. PMID: 11062480

6

The CEPH consortium linkage map of human chromosome 2.

Spurr NK, Cox S, Bryant SP, Attwood J, Robson EB, Shields DC, Steinbrueck T, Jenkins T, Murray JC, Kidd KK, et al. Spurr NK, et al. Among authors: jenkins t. Genomics. 1992 Dec;14(4):1055-63. doi: 10.1016/s0888-7543(05)80129-6. Genomics. 1992. PMID: 1478647

7

A new negroid-specific HindIII polymorphism in the serum amyloid A1 (SAA1) gene increases the usefulness of the SAA locus in linkage studies.

Stevens G, Ramsay M, Kluve-Beckerman B, Jenkins T. Stevens G, et al. Among authors: jenkins t. Genomics. 1993 Jan;15(1):242-3. doi: 10.1006/geno.1993.1050. Genomics. 1993. PMID: 8094371 No abstract available.

8

The CEPH consortium linkage map of human chromosome 15q.

Bowcock AM, Barnes RI, White RL, Kruse TA, Tsipouras P, Sarfarazi M, Jenkins T, Viljoen C, Litt M, Kramer PL, et al. Bowcock AM, et al. Among authors: jenkins t. Genomics. 1992 Dec;14(4):833-40. doi: 10.1016/s0888-7543(05)80101-6. Genomics. 1992. PMID: 1478662

9

An arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4.

Verga V, Dos Santos M, Marques I, Povey S, Ramsay M, Jenkins T. Verga V, et al. Among authors: jenkins t. Nucleic Acids Res. 1989 Jul 11;17(13):5423. doi: 10.1093/nar/17.13.5423. Nucleic Acids Res. 1989. PMID: 2569718 Free PMC article.

10

An arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4].

Verga V, Dos Santos M, Marques I, Povey S, Ramsay M, Jenkins T. Verga V, et al. Among authors: jenkins t. Nucleic Acids Res. 1989 May 25;17(10):4010. doi: 10.1093/nar/17.10.4010. Nucleic Acids Res. 1989. PMID: 2567510 Free PMC article.

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