These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

74 related articles for article (PubMed ID: 1303248)

  • 1. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.
    Murray JC; Bennett SR; Kwitek AE; Small KW; Schinzel A; Alward WL; Weber JL; Bell GI; Buetow KH
    Nat Genet; 1992 Sep; 2(1):46-9. PubMed ID: 1303248
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rieger syndrome revisited: experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-alpha functions resulting in dysmorphogenesis during embryonic mouse craniofacial morphogenesis.
    Slavkin HC
    Am J Med Genet; 1993 Oct; 47(5):689-97; discussion 687-8. PubMed ID: 8266997
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A genetic analysis of the Werner syndrome region on human chromosome 8p.
    Thomas W; Rubenstein M; Goto M; Drayna D
    Genomics; 1993 Jun; 16(3):685-90. PubMed ID: 8325642
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).
    Makita Y; Masuno M; Imaizumi K; Yamashita S; Ohba S; Ito D; Kuroki Y
    Am J Med Genet; 1995 May; 57(1):19-21. PubMed ID: 7645592
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this gene.
    Flomen RH; Vatcheva R; Gorman PA; Baptista PR; Groet J; Barisić I; Ligutic I; Nizetić D
    Genomics; 1998 Feb; 47(3):409-13. PubMed ID: 9480756
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Polymorphic SSR (simple-sequence-repeat) markers for chromosome 20.
    Melis R; Bradley P; Elsner T; Robertson M; Lawrence E; Gerken S; Albertsen H; White R
    Genomics; 1993 Apr; 16(1):56-62. PubMed ID: 8486385
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.
    Diaz GA; Khan KT; Gelb BD
    Genomics; 1998 Nov; 54(1):13-8. PubMed ID: 9806825
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Conserved synteny between pig chromosome 8 and human chromosome 4 but rearranged and distorted linkage maps.
    Ellegren H; Fredholm M; Edfors-Lilja I; Winterø AK; Andersson L
    Genomics; 1993 Sep; 17(3):599-603. PubMed ID: 8244376
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The ovine Booroola fecundity gene (FecB) is linked to markers from a region of human chromosome 4q.
    Montgomery GW; Crawford AM; Penty JM; Dodds KG; Ede AJ; Henry HM; Pierson CA; Lord EA; Galloway SM; Schmack AE
    Nat Genet; 1993 Aug; 4(4):410-4. PubMed ID: 8401591
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
    Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.
    Todd S; Sherman SL; Naylor SL
    Genomics; 1993 Jun; 16(3):612-8. PubMed ID: 8100800
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Linkage of congenital isolated adrenocorticotropic hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms.
    Kyllo JH; Collins MM; Vetter KL; Cuttler L; Rosenfield RL; Donohoue PA
    Am J Med Genet; 1996 Mar; 62(3):262-7. PubMed ID: 8882784
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.
    Kumar S; Kimberling WJ; Lanyi A; Sumegi J; Pinnt J; Ing P; Tinley S; Marres HA; Cremers CW
    Genomics; 1996 Jan; 31(1):71-9. PubMed ID: 8808282
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene.
    Biancalana V; Trivier E; Weber C; Weissenbach J; Rowe PS; O'Riordan JL; Partington MW; Heyberger S; Oudet C; Hanauer A
    Genomics; 1994 Aug; 22(3):617-25. PubMed ID: 8001973
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exclusion of linkage between alcoholism and the MNS blood group region on chromosome 4q in multiplex families.
    Neiswanger K; Kaplan B; Hill SY
    Am J Med Genet; 1995 Feb; 60(1):72-9. PubMed ID: 7485239
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.
    Watanabe Y; Murray JC; Bjork BC; Bird CP; Chiang PW; Gregory SG; Kurnit DM; Schutte BC
    Hum Mutat; 2001 Nov; 18(5):422-34. PubMed ID: 11668635
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
    Tsukurov O; Boehmer A; Flynn J; Nicolai JP; Hamel BC; Traill S; Zaleske D; Mankin HJ; Yeon H; Ho C
    Nat Genet; 1994 Mar; 6(3):282-6. PubMed ID: 8012391
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.
    Leppert M; Baird L; Anderson KL; Otterud B; Lupski JR; Lewis RA
    Nat Genet; 1994 May; 7(1):108-12. PubMed ID: 8075632
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.