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Items: 1 to 20 of 248

1.

Comprehensive human genetic maps: individual and sex-specific variation in recombination.

Broman KW, Murray JC, Sheffield VC, White RL, Weber JL.

Am J Hum Genet. 1998 Sep;63(3):861-9.

2.

Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.

Weber JL, Wang Z, Hansen K, Stephenson M, Kappel C, Salzman S, Wilkie PJ, Keats B, Dracopoli NC, Brandriff BF, et al.

Am J Hum Genet. 1993 Nov;53(5):1079-95.

3.
4.

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps.

Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, et al.

Hum Mol Genet. 1995 Oct;4(10):1837-44.

PMID:
8595404
5.

Physical and genetic maps for chromosome 10.

Lichter JB, Difilippantonio MJ, Pakstis AJ, Goodfellow PJ, Ward DC, Kidd KK.

Genomics. 1993 May;16(2):320-4.

PMID:
8314570
6.

Report of the first workshop on the genetic map of bovine chromosome 23.

Beever JE, Lewin HA, Barendse W, Andersson L, Armitage SM, Beattie CW, Burns BM, Davis SK, Kappes SM, Kirkpatrick BW, Ma RZ, McGraw RA, Stone RT, Taylor JF.

Anim Genet. 1996 Apr;27(2):69-75.

PMID:
8856895
7.

Integrated genetic map of human chromosome 2.

Cox S, Bryant SP, Collins A, Weissenbach J, Donis-Keller H, Koeleman BP, Steinkasserer A, Spurr NK.

Ann Hum Genet. 1995 Oct;59(Pt 4):413-34.

PMID:
8579334
8.

Polymorphic markers for the arylsulfatase A gene reveal a greatly expanded meiotic map for the human 22q telomeric region.

Brennan MD, Neibergs HL, Phillips K, Moseley S.

Genomics. 2000 Feb 1;63(3):430-2.

PMID:
10704291
9.

Susceptibility genes for nicotine dependence: a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further study.

Straub RE, Sullivan PF, Ma Y, Myakishev MV, Harris-Kerr C, Wormley B, Kadambi B, Sadek H, Silverman MA, Webb BT, Neale MC, Bulik CM, Joyce PR, Kendler KS.

Mol Psychiatry. 1999 Mar;4(2):129-44.

PMID:
10208445
10.

Linkage genome scan for loci predisposing to panic disorder or agoraphobia.

Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.

Am J Med Genet. 2001 Aug 8;105(6):548-57.

PMID:
11496373
11.

Genetic mapping of the erythropoietin receptor gene.

Sistonen P, Träskelin AL, Lehväslaiho H, de la Chapelle A.

Hum Genet. 1993 Oct 1;92(3):299-301.

PMID:
8406437
12.
13.

A microsatellite-based multipoint index map of human chromosome 22.

Buetow KH, Duggan D, Yang B, Ludwigsen S, Puck J, Porter J, Budarf M, Spielman R, Emanuel BS.

Genomics. 1993 Nov;18(2):329-39.

PMID:
8288236
14.

A discordant sib-pair linkage analysis of age-related macular degeneration.

Santangelo SL, Yen CH, Haddad S, Fagerness J, Huang C, Seddon JM.

Ophthalmic Genet. 2005 Jun;26(2):61-7.

PMID:
16020308
15.

The fine-scale structure of recombination rate variation in the human genome.

McVean GA, Myers SR, Hunt S, Deloukas P, Bentley DR, Donnelly P.

Science. 2004 Apr 23;304(5670):581-4.

16.

A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature.

Deng HW, Xu FH, Liu YZ, Shen H, Deng H, Huang QY, Liu YJ, Conway T, Li JL, Davies KM, Recker RR.

Am J Med Genet. 2002 Nov 15;113(1):29-39.

PMID:
12400063
17.

Location on the human genetic linkage map of 26 genes involved in blood coagulation.

Koeleman BP, Reitsma PH, Bakker E, Bertina RM.

Thromb Haemost. 1997 May;77(5):873-8.

PMID:
9184395
18.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.

Mol Psychiatry. 2007 Apr;12(4):376-84. Epub 2006 Dec 19.

PMID:
17179998
19.
20.

Microsatellite polymorphisms and the genetic linkage map of the human genome.

Weissenbach J.

Curr Opin Genet Dev. 1993 Jun;3(3):414-7. Review.

PMID:
8353415

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