172 related articles for article (PubMed ID: 9299238)
1. A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.
Baysal BE; van Schothorst EM; Farr JE; James MR; Devilee P; Richard CW
Genomics; 1997 Sep; 44(2):214-21. PubMed ID: 9299238
[TBL] [Abstract][Full Text] [Related]
2. A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.
Baysal BE; Willett-Brozick JE; Taschner PE; Dauwerse JG; Devilee P; Devlin B
Eur J Hum Genet; 2001 Feb; 9(2):121-9. PubMed ID: 11313745
[TBL] [Abstract][Full Text] [Related]
3. Defining a common region of deletion at 13q21 in human cancers.
Chen C; Brabham WW; Stultz BG; Frierson HF; Barrett JC; Sawyers CL; Isaacs JT; Dong JT
Genes Chromosomes Cancer; 2001 Aug; 31(4):333-44. PubMed ID: 11433524
[TBL] [Abstract][Full Text] [Related]
4. A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p).
Baens M; Wlodarska I; Corveleyn A; Hoornaert I; Hagemeijer A; Marynen P
Genomics; 1999 Feb; 56(1):40-50. PubMed ID: 10036184
[TBL] [Abstract][Full Text] [Related]
5. Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
Mohlke KL; Purkayastha AA; Westrick RJ; Ginsburg D
Genomics; 1998 Nov; 54(1):19-30. PubMed ID: 9806826
[TBL] [Abstract][Full Text] [Related]
6. Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22.
Bolino A; Levy ER; Muglia M; Conforti FL; LeGuern E; Salih MA; Georgiou DM; Christodoulou RK; Hausmanowa-Petrusewicz I; Mandich P; Gambardella A; Quattrone A; Devoto M; Monaco AP
Genomics; 2000 Jan; 63(2):271-8. PubMed ID: 10673338
[TBL] [Abstract][Full Text] [Related]
7. A sequence-ready BAC clone contig of human chromosome 10p15 spanning the loss of heterozygosity region in glioma.
Harada K; Nishizaki T; Maekawa K; Kubota H; Harada K; Suzuki M; Ohno T; Sasaki K; Soeda E
Genomics; 2000 Aug; 67(3):268-72. PubMed ID: 10936048
[TBL] [Abstract][Full Text] [Related]
8. An integrated genetic and physical map of the autosomal recessive polycystic kidney disease region.
Lens XM; Onuchic LF; Wu G; Hayashi T; Daoust M; Mochizuki T; Santarina LB; Stockwin JM; Mücher G; Becker J; Sweeny WE; Avner ED; Guay-Woodford L; Zerres K; Somlo S; Germino GG
Genomics; 1997 May; 41(3):463-6. PubMed ID: 9169147
[TBL] [Abstract][Full Text] [Related]
9. A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.
Machado RD; Pauciulo MW; Fretwell N; Veal C; Thomson JR; Vilariño Güell C; Aldred M; Brannon CA; Trembath RC; Nichols WC
Genomics; 2000 Sep; 68(2):220-8. PubMed ID: 10964520
[TBL] [Abstract][Full Text] [Related]
10. A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene.
Irobi J; Tissir F; De Jonghe P; De Vriendt E; Van Broeckhoven C; Timmerman V; Beuten J
Genomics; 2000 Apr; 65(1):34-43. PubMed ID: 10777663
[TBL] [Abstract][Full Text] [Related]
11. An EST and STS-based YAC contig map of human chromosome 9q22.3.
Lench NJ; Telford EA; Andersen SE; Moynihan TP; Robinson PA; Markham AF
Genomics; 1996 Dec; 38(2):199-205. PubMed ID: 8954802
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.
Wilgenbus KK; Seranski P; Brown A; Leuchs B; Mincheva A; Lichter P; Poustka A
Genomics; 1997 May; 42(1):1-10. PubMed ID: 9177769
[TBL] [Abstract][Full Text] [Related]
13. Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.
Eisenberg I; Hochner H; Shemesh M; Levi T; Potikha T; Sadeh M; Argov Z; Jackson CL; Mitrani-Rosenbaum S
Eur J Hum Genet; 2001 Jul; 9(7):501-9. PubMed ID: 11464241
[TBL] [Abstract][Full Text] [Related]
14. A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes.
Rozenblum E; Vahteristo P; Sandberg T; Bergthorsson JT; Syrjakoski K; Weaver D; Haraldsson K; Johannsdottir HK; Vehmanen P; Nigam S; Golberger N; Robbins C; Pak E; Dutra A; Gillander E; Stephan DA; Bailey-Wilson J; Juo SH; Kainu T; Arason A; Barkardottir RB; Nevanlinna H; Borg A; Kallioniemi OP
Hum Genet; 2002 Feb; 110(2):111-21. PubMed ID: 11935316
[TBL] [Abstract][Full Text] [Related]
15. A panel of sequence tagged sites for chromosome band 11q23.
Tunnacliffe A; Perry H; Radice P; Budarf ML; Emanuel BS
Genomics; 1993 Sep; 17(3):744-7. PubMed ID: 8244392
[TBL] [Abstract][Full Text] [Related]
16. A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.
Kuhlenbäumer G; Schirmacher A; Meuleman J; Tissir F; Del-Favero J; Stögbauer F; Young P; Ringelstein B; Van Broeckhoven C; Timmerman V
Genomics; 1999 Dec; 62(2):242-50. PubMed ID: 10610718
[TBL] [Abstract][Full Text] [Related]
17. Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21.
Kärrman C; Bäckman B; Dixon M; Holmgren G; Forsman K
Genomics; 1997 Jan; 39(2):164-70. PubMed ID: 9027503
[TBL] [Abstract][Full Text] [Related]
18. A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 region.
Mitsuda N; Nakura J; Ye L; Zhao Y; Fujioka Y; Takahashi-Fujii A; Ishino Y; Kato I; Hashimoto K; Ogihara T; Miki T
Genomics; 1997 Apr; 41(1):49-55. PubMed ID: 9126481
[TBL] [Abstract][Full Text] [Related]
19. A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11.
Lamartine J; Pitaval A; Soularue P; Lanneluc I; Lemaître G; Kibar Z; Rouleau GA; Waksman G
Genomics; 2000 Jul; 67(2):232-6. PubMed ID: 10903849
[TBL] [Abstract][Full Text] [Related]
20. Construction of a 5-Mb YAC contig from the putative 10q25 tumor-suppressor region for glioblastomas.
Albarosa R; Finocchiaro G; Chiariello E; Russo G; Susani L; Vezzoni P; Zucchi I
Genomics; 1997 May; 41(3):345-9. PubMed ID: 9169131
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
