BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

354 related articles for article (PubMed ID: 1639385)

  • 1. Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p.
    Guzzetta V; Franco B; Trask BJ; Zhang H; Saucedo-Cardenas O; Montes de Oca-Luna R; Greenberg F; Chinault AC; Lupski JR; Patel PI
    Genomics; 1992 Jul; 13(3):551-9. PubMed ID: 1639385
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients.
    Juyal RC; Figuera LE; Hauge X; Elsea SH; Lupski JR; Greenberg F; Baldini A; Patel PI
    Am J Hum Genet; 1996 May; 58(5):998-1007. PubMed ID: 8651284
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).
    Greenberg F; Guzzetta V; Montes de Oca-Luna R; Magenis RE; Smith AC; Richter SF; Kondo I; Dobyns WB; Patel PI; Lupski JR
    Am J Hum Genet; 1991 Dec; 49(6):1207-18. PubMed ID: 1746552
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome.
    Chevillard C; Le Paslier D; Passage E; Ougen P; Billault A; Boyer S; Mazan S; Bachellerie JP; Vignal A; Cohen D
    Hum Mol Genet; 1993 Aug; 2(8):1235-43. PubMed ID: 8401506
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two patients with duplication of 17p11.2: the reciprocal of the Smith-Magenis syndrome deletion?
    Brown A; Phelan MC; Patil S; Crawford E; Rogers RC; Schwartz C
    Am J Med Genet; 1996 May; 63(2):373-7. PubMed ID: 8725788
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome.
    Moncla A; Piras L; Arbex OF; Muscatelli F; Mattei MG; Mattei JF; Fontes M
    Hum Genet; 1993 Feb; 90(6):657-60. PubMed ID: 8444473
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Structure and evolution of the Smith-Magenis syndrome repeat gene clusters, SMS-REPs.
    Park SS; Stankiewicz P; Bi W; Shaw C; Lehoczky J; Dewar K; Birren B; Lupski JR
    Genome Res; 2002 May; 12(5):729-38. PubMed ID: 11997339
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23.
    McConville CM; Byrd PJ; Ambrose HJ; Stankovic T; Ziv Y; Bar-Shira A; Vanagaite L; Rotman G; Shiloh Y; Gillett GT
    Hum Mol Genet; 1993 Jul; 2(7):969-74. PubMed ID: 8364579
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion.
    Potocki L; Chen KS; Park SS; Osterholm DE; Withers MA; Kimonis V; Summers AM; Meschino WS; Anyane-Yeboa K; Kashork CD; Shaffer LG; Lupski JR
    Nat Genet; 2000 Jan; 24(1):84-7. PubMed ID: 10615134
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10.
    Zheng CJ; Ma NS; Dorman TE; Wang MT; Braunschweiger K; Soares L; Schuster MK; Rothschild CB; Bowden DW; Torrey D
    Genomics; 1994 Jul; 22(1):55-67. PubMed ID: 7959792
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patient with large 17p11.2 deletion presenting with Smith-Magenis syndrome and Joubert syndrome phenotype.
    Natacci F; Corrado L; Pierri M; Rossetti M; Zuccarini C; Riva P; Miozzo M; Larizza L
    Am J Med Genet; 2000 Dec; 95(5):467-72. PubMed ID: 11146468
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A radiation hybrid map of human chromosome 18.
    Francke U; Chang E; Comeau K; Geigl EM; Giacalone J; Li X; Luna J; Moon A; Welch S; Wilgenbus P
    Cytogenet Cell Genet; 1994; 66(3):196-213. PubMed ID: 8125019
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.
    Bi W; Park SS; Shaw CJ; Withers MA; Patel PI; Lupski JR
    Am J Hum Genet; 2003 Dec; 73(6):1302-15. PubMed ID: 14639526
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts.
    Kere J; Nagaraja R; Mumm S; Ciccodicola A; D'Urso M; Schlessinger D
    Genomics; 1992 Oct; 14(2):241-8. PubMed ID: 1427839
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.
    Glaser T; Housman D; Lewis WH; Gerhard D; Jones C
    Somat Cell Mol Genet; 1989 Nov; 15(6):477-501. PubMed ID: 2595451
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Assignment of developmentally regulated GTP-binding protein (DRG2) to human chromosome band 17p11.2 with somatic cell hybrids and localization to the Smith-Magenis syndrome critical interval.
    Vlangos CN; Das P; Patel PI; Elsea SH
    Cytogenet Cell Genet; 2000; 88(3-4):283-5. PubMed ID: 10828610
    [No Abstract]   [Full Text] [Related]  

  • 18. Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites.
    Richards RI; Holman K; Lane S; Sutherland GR; Callen DF
    Genomics; 1991 Aug; 10(4):1047-52. PubMed ID: 1916811
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.
    Juyal RC; Kuwano A; Kondo I; Zara F; Baldini A; Patel PI
    Am J Med Genet; 1996 Dec; 66(2):193-6. PubMed ID: 8958329
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library.
    Driesen MS; Dauwerse JG; Wapenaar MC; Meershoek EJ; Mollevanger P; Chen KL; Fischbeck KH; van Ommen GJ
    Genomics; 1991 Dec; 11(4):1079-87. PubMed ID: 1783377
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.