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 *

126 related articles for article (PubMed ID: 9195154)

  • 1. Characterisation of X;17(q12;p13) translocation breakpoints in a female patient with hypomelanosis of Ito and choroid plexus papilloma.
    Zajac V; Kirchhoff T; Levy ER; Horsley SW; Miller A; Steichen-Gersdorf E; Monaco AP
    Eur J Hum Genet; 1997; 5(2):61-8. PubMed ID: 9195154
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.
    Bienvenu T; Der-Sarkissian H; Billuart P; Tissot M; Des Portes V; Brüls T; Chabrolle JP; Chauveau P; Cherry M; Kahn A; Cohen D; Beldjord C; Chelly J; Cherif D
    Eur J Hum Genet; 1997; 5(2):105-9. PubMed ID: 9195162
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25.
    Ladanyi M; Lui MY; Antonescu CR; Krause-Boehm A; Meindl A; Argani P; Healey JH; Ueda T; Yoshikawa H; Meloni-Ehrig A; Sorensen PH; Mertens F; Mandahl N; van den Berghe H; Sciot R; Dal Cin P; Bridge J
    Oncogene; 2001 Jan; 20(1):48-57. PubMed ID: 11244503
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hypomelanosis of Ito in a girl with plexus papilloma and translocation (X;17).
    Steichen-Gersdorf E; Trawöger R; Duba HC; Mayr U; Felber S; Utermann G
    Hum Genet; 1993 Feb; 90(6):611-3. PubMed ID: 8444466
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.
    De Baere E; Van Roy N; Speleman F; Fukushima Y; De Paepe A; Messiaen L
    Genomics; 1999 Apr; 57(1):70-8. PubMed ID: 10191085
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
    Gorski JL; Bialecki MD; McDonald MT; Massa HF; Trask BJ; Burright EN
    Genomics; 1996 Jul; 35(2):338-45. PubMed ID: 8661147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes.
    Seranski P; Heiss NS; Dhorne-Pollet S; Radelof U; Korn B; Hennig S; Backes E; Schmidt S; Wiemann S; Schwarz CE; Lehrach H; Poustka A
    Genomics; 1999 Feb; 56(1):1-11. PubMed ID: 10036180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypomelanosis of Ito associated with chromosomal translocation involving Xp11.
    Lungarotti MS; Martello C; Calabro A; Baldari F; Mariotti G
    Am J Med Genet; 1991 Sep; 40(4):447-8. PubMed ID: 1746610
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
    Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
    Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
    Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
    Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal evaluation of a de novo X;9 translocation.
    Feldman B; Kramer RL; Ebrahim SA; Wolff DJ; Evans MI
    Am J Med Genet; 1999 Aug; 85(5):476-8. PubMed ID: 10405445
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A translocation interrupts the COL5A1 gene in a patient with Ehlers-Danlos syndrome and hypomelanosis of Ito.
    Toriello HV; Glover TW; Takahara K; Byers PH; Miller DE; Higgins JV; Greenspan DS
    Nat Genet; 1996 Jul; 13(3):361-5. PubMed ID: 8673139
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
    McDonell N; Ramser J; Francis F; Vinet MC; Rider S; Sudbrak R; Riesselman L; Yaspo ML; Reinhardt R; Monaco AP; Ross F; Kahn A; Kearney L; Buckle V; Chelly J
    Genomics; 2000 Mar; 64(3):221-9. PubMed ID: 10756090
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
    Murga Penas EM; Cools J; Algenstaedt P; Hinz K; Seeger D; Schafhausen P; Schilling G; Marynen P; Hossfeld DK; Dierlamm J
    Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11.
    Koiffmann CP; de Souza DH; Diament A; Ventura HB; Alves RS; Kihara S; Wajntal A
    Am J Med Genet; 1993 Jun; 46(5):529-33. PubMed ID: 8322815
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA).
    Thomas NS; Chelly J; Zonana J; Davies KJ; Morgan S; Gault J; Rack KA; Buckle VJ; Brockdorff N; Clarke A
    Hum Mol Genet; 1993 Oct; 2(10):1679-85. PubMed ID: 8268921
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.
    Popovici C; Basset C; Bertucci F; Orsetti B; Adélaide J; Mozziconacci MJ; Conte N; Murati A; Ginestier C; Charafe-Jauffret E; Ethier SP; Lafage-Pochitaloff M; Theillet C; Birnbaum D; Chaffanet M
    Genes Chromosomes Cancer; 2002 Nov; 35(3):204-18. PubMed ID: 12353263
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
    Verkerk AJ; Pieretti M; Sutcliffe JS; Fu YH; Kuhl DP; Pizzuti A; Reiner O; Richards S; Victoria MF; Zhang FP
    Cell; 1991 May; 65(5):905-14. PubMed ID: 1710175
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation.
    Zemni R; Bienvenu T; Vinet MC; Sefiani A; Carrié A; Billuart P; McDonell N; Couvert P; Francis F; Chafey P; Fauchereau F; Friocourt G; des Portes V; Cardona A; Frints S; Meindl A; Brandau O; Ronce N; Moraine C; van Bokhoven H; Ropers HH; Sudbrak R; Kahn A; Fryns JP; Beldjord C; Chelly J
    Nat Genet; 2000 Feb; 24(2):167-70. PubMed ID: 10655063
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization and mapping to human chromosome 8q24.3 of Ly-6-related gene 9804 encoding an apparent homologue of mouse TSA-1.
    Shan X; Bourdeau A; Rhoton A; Wells DE; Cohen EH; Landgraf BE; Palfree RG
    J Immunol; 1998 Jan; 160(1):197-208. PubMed ID: 9551972
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.