BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 7521123)

  • 1. Six cases of 7p deletion: clinical, cytogenetic, and molecular studies.
    Chotai KA; Brueton LA; van Herwerden L; Garrett C; Hinkel GK; Schinzel A; Mueller RF; Speleman F; Winter RM
    Am J Med Genet; 1994 Jul; 51(3):270-6. PubMed ID: 7521123
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Craniosynostosis and hemizygosity for D7S135 caused by a de novo and apparently balanced t(6;7) translocation.
    Tsuji K; Narahara K; Kikkawa K; Murakami M; Yokoyama Y; Ninomiya S; Seino Y
    Am J Med Genet; 1994 Jan; 49(1):98-102. PubMed ID: 7909651
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization of genes and anonymous DNA probes on the short arm of chromosome 7.
    Wagner K; Kroisel PM; Rosenkranz W
    Mamm Genome; 1992; 3(1):39-41. PubMed ID: 1316194
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.
    Aughton DJ; Cassidy SB; Whiteman DA; Delach JA; Guttmacher AE
    Am J Med Genet; 1991 Sep; 40(4):440-3. PubMed ID: 1746608
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 7p deletion syndrome: an adult with mild manifestations.
    Grebe TA; Stevens MA; Byrne-Essif K; Cassidy SB
    Am J Med Genet; 1992 Sep; 44(1):18-23. PubMed ID: 1519644
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.
    Shetty S; Boycott KM; Gillan TL; Bowser K; Parboosingh JS; McInnes B; Chernos JE; Bernier FP
    Clin Dysmorphol; 2007 Oct; 16(4):253-6. PubMed ID: 17786117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo del(7)(pter----p21.2::p15.2----qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndrome.
    García-Esquivel L; García-Cruz D; Rivera H; Plascencia ML; Cantú JM
    Ann Genet; 1986; 29(1):36-8. PubMed ID: 3487273
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
    Fryns JP; Haspeslagh M; Agneessens A; van den Berghe H
    Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
    Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.
    Vortkamp A; Gessler M; Grzeschik KH
    Nature; 1991 Aug; 352(6335):539-40. PubMed ID: 1650914
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acute lymphoblastic leukemia in a patient with Greig cephalopolysyndactyly and interstitial deletion of chromosome 7 del(7)(p11.2 p14) involving the GLI3 and ZNFN1A1 genes.
    Mendoza-Londono R; Kashork CD; Shaffer LG; Krance R; Plon SE
    Genes Chromosomes Cancer; 2005 Jan; 42(1):82-6. PubMed ID: 15390181
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p.
    Vortkamp A; Thias U; Gessler M; Rosenkranz W; Kroisel PM; Tommerup N; Krüger G; Götz J; Pelz L; Grzeschik KH
    Genomics; 1991 Nov; 11(3):737-43. PubMed ID: 1663489
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytogenetic and molecular analysis in Angelman syndrome.
    Zackowski JL; Nicholls RD; Gray BA; Bent-Williams A; Gottlieb W; Harris PJ; Waters MF; Driscoll DJ; Zori RT; Williams CA
    Am J Med Genet; 1993 Apr; 46(1):7-11. PubMed ID: 8098583
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS).
    Schwarzbraun T; Windpassinger C; Ofner L; Vincent JB; Cheung J; Scherer SW; Wagner K; Kroisel PM; Petek E
    Eur J Med Genet; 2006; 49(4):338-45. PubMed ID: 16829355
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [7p-deletion syndrome].
    Hinkel GK; Tolkendorf E; Bergan J
    Monatsschr Kinderheilkd; 1988 Dec; 136(12):824-7. PubMed ID: 3237228
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies.
    Brezinová J; Zemanová Z; Ransdorfová S; Pavlistová L; Babická L; Housková L; Melichercíková J; Sisková M; Cermák J; Michalová K
    Cancer Genet Cytogenet; 2007 Feb; 173(1):10-6. PubMed ID: 17284364
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes.
    Wagner K; Kroisel PM; Rosenkranz W
    Genomics; 1990 Nov; 8(3):487-91. PubMed ID: 1981052
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
    Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.
    Shannon KM; Turhan AG; Chang SS; Bowcock AM; Rogers PC; Carroll WL; Cowan MJ; Glader BE; Eaves CJ; Eaves AC
    J Clin Invest; 1989 Sep; 84(3):984-9. PubMed ID: 2569483
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.
    Pettigrew AL; Greenberg F; Caskey CT; Ledbetter DH
    Hum Genet; 1991 Aug; 87(4):452-6. PubMed ID: 1879832
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.