162 related articles for article (PubMed ID: 7802004)
1. Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndrome.
Edery P; Manach Y; Le Merrer M; Till M; Vignal A; Lyonnet S; Munnich A
Am J Med Genet; 1994 Aug; 52(2):174-7. PubMed ID: 7802004
[TBL] [Abstract][Full Text] [Related]
2. Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3.
Jabs EW; Li X; Coss CA; Taylor EW; Meyers DA; Weber JL
Genomics; 1991 Sep; 11(1):193-8. PubMed ID: 1765376
[TBL] [Abstract][Full Text] [Related]
3. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
Rosen DR; Sapp P; O'Regan J; McKenna-Yasek D; Schlumpf KS; Haines JL; Gusella JF; Horvitz HR; Brown RH
Am J Med Genet; 1994 May; 51(1):61-9. PubMed ID: 7913294
[TBL] [Abstract][Full Text] [Related]
4. Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2.
Dixon MJ; Dixon J; Raskova D; Le Beau MM; Williamson R; Klinger K; Landes GM
Hum Mol Genet; 1992 Jul; 1(4):249-53. PubMed ID: 1303194
[TBL] [Abstract][Full Text] [Related]
5. Treacher Collins syndrome: correlation between clinical and genetic linkage studies.
Dixon MJ; Marres HA; Edwards SJ; Dixon J; Cremers CW
Clin Dysmorphol; 1994 Apr; 3(2):96-103. PubMed ID: 8055143
[TBL] [Abstract][Full Text] [Related]
6. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
Bruford EA; Riise R; Teague PW; Porter K; Thomson KL; Moore AT; Jay M; Warburg M; Schinzel A; Tommerup N; Tornqvist K; Rosenberg T; Patton M; Mansfield DC; Wright AF
Genomics; 1997 Apr; 41(1):93-9. PubMed ID: 9126487
[TBL] [Abstract][Full Text] [Related]
7. Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group.
Nat Genet; 1996 Feb; 12(2):130-6. PubMed ID: 8563749
[TBL] [Abstract][Full Text] [Related]
8. Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1.
Dixon MJ; Dixon J; Houseal T; Bhatt M; Ward DC; Klinger K; Landes GM
Am J Hum Genet; 1993 May; 52(5):907-14. PubMed ID: 8488840
[TBL] [Abstract][Full Text] [Related]
9. Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 region.
Jabs EW; Li X; Lovett M; Yamaoka LH; Taylor E; Speer MC; Coss C; Cadle R; Hall B; Brown K
Genomics; 1993 Oct; 18(1):7-13. PubMed ID: 8276417
[TBL] [Abstract][Full Text] [Related]
10. The gene for Treacher Collins syndrome maps to the long arm of chromosome 5.
Dixon MJ; Read AP; Donnai D; Colley A; Dixon J; Williamson R
Am J Hum Genet; 1991 Jul; 49(1):17-22. PubMed ID: 1676560
[TBL] [Abstract][Full Text] [Related]
11. A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.
Preston RA; Post JC; Keats BJ; Aston CE; Ferrell RE; Priest J; Nouri N; Losken HW; Morris CA; Hurtt MR
Nat Genet; 1994 Jun; 7(2):149-53. PubMed ID: 7920632
[TBL] [Abstract][Full Text] [Related]
12. Potential linkage for schizophrenia on chromosome 22q12-q13: a replication study.
Schwab SG; Lerer B; Albus M; Maier W; Hallmayer J; Fimmers R; Lichtermann D; Minges J; Bondy B; Ackenheil M
Am J Med Genet; 1995 Oct; 60(5):436-43. PubMed ID: 8546158
[TBL] [Abstract][Full Text] [Related]
13. Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1.
Hedera P; Toriello HV; Petty EM
J Med Genet; 2002 Jul; 39(7):484-8. PubMed ID: 12114479
[TBL] [Abstract][Full Text] [Related]
14. Clinical features, treatment and genetic background of Treacher Collins syndrome.
Marszałek B; Wójcicki P; Kobus K; Trzeciak WH
J Appl Genet; 2002; 43(2):223-33. PubMed ID: 12080178
[TBL] [Abstract][Full Text] [Related]
15. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
McKay JD; Patterson B; Craig JE; Russell-Eggitt IM; Wirth MG; Burdon KP; Hewitt AW; Cohn AC; Kerdraon Y; Mackey DA
Br J Ophthalmol; 2005 Jul; 89(7):831-4. PubMed ID: 15965161
[TBL] [Abstract][Full Text] [Related]
16. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
Lohmann-Hedrich K; Neumann A; Kleensang A; Lohnau T; Muhle H; Djarmati A; König IR; Pramstaller PP; Schwinger E; Kramer PL; Ziegler A; Stephani U; Klein C
Neurology; 2008 Feb; 70(9):686-94. PubMed ID: 18032746
[TBL] [Abstract][Full Text] [Related]
17. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.
Pang CP; Fan BJ; Canlas O; Wang DY; Dubois S; Tam PO; Lam DS; Raymond V; Ritch R
Mol Vis; 2006 Feb; 12():85-92. PubMed ID: 16518310
[TBL] [Abstract][Full Text] [Related]
18. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
Xia J; Deng H; Feng Y; Zhang H; Pan Q; Dai H; Long Z; Tang B; Deng H; Chen Y; Zhang R; Zheng D; He Y; Xia K
J Hum Genet; 2002; 47(12):635-40. PubMed ID: 12522684
[TBL] [Abstract][Full Text] [Related]
19. Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.
Jordan SA; Farrar GJ; Kenna P; Humphries MM; Sheils DM; Kumar-Singh R; Sharp EM; Soriano N; Ayuso C; Benitez J
Nat Genet; 1993 May; 4(1):54-8. PubMed ID: 8513324
[TBL] [Abstract][Full Text] [Related]
20. Evidence that a gene for essential tremor maps to chromosome 2p in four families.
Higgins JJ; Loveless JM; Jankovic J; Patel PI
Mov Disord; 1998 Nov; 13(6):972-7. PubMed ID: 9827627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
