BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 6680318)

  • 1. An additional case of 9p syndrome.
    Latos-Bielenska A; Krawczynski M; Ignys I; Wolnik-Brzozowska D
    Acta Anthropogenet; 1983; 7(4):391-5. PubMed ID: 6680318
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The 9p- syndrome.
    Alfi OS; Donnell GN; Allderdice PW; Derencsenyi A
    Ann Genet; 1976 Mar; 19(1):11-6. PubMed ID: 1084115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
    Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
    Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A clinical syndrome associated with 5p duplication and 9p deletion.
    Liberfarb RM; Atkins L; Holmes LB
    Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Brief clinical report: two children with de novo del(9p).
    Young RS; Bader P; Palmer CG; Kaler SG; Hodes ME
    Am J Med Genet; 1983 Apr; 14(4):751-7. PubMed ID: 6846405
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 9p-Syndrome.
    Boby J; Karande SC; Lahiri KR; Jain MK; Kanade S
    J Postgrad Med; 1994; 40(1):40-1. PubMed ID: 8568717
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosome 6q- and associated malformations.
    Liberfarb RM; Atkins L; Holmes LB
    Ann Genet; 1978 Dec; 21(4):223-5. PubMed ID: 314259
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21).
    Holden JJ; MacDonald EA
    Am J Med Genet; 1985 Feb; 20(2):245-8. PubMed ID: 2579554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further delineation of the 10p deletion syndrome.
    Elstner CL; Carey JC; Livingston G; Moeschler J; Lubinsky M
    Pediatrics; 1984 May; 73(5):670-5. PubMed ID: 6718125
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
    Martin-Pont B; Pilczer C; Dandine M; Tamboise A
    Ann Genet; 1985; 28(4):251-3. PubMed ID: 3879441
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Trigonocephaly and the 11q- syndrome.
    Cassidy SB; Heller RM; Kilroy AW; McKelvey W; Engel E
    Ann Genet; 1977 Mar; 20(1):67-9. PubMed ID: 302679
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Terminal deletion of the short arm of chromosome 3, del(3pter-p25): a recognizable syndrome.
    Schwyzer U; Binkert F; Caflisch U; Baumgartner B; Schinzel A
    Helv Paediatr Acta; 1987; 42(4):309-15. PubMed ID: 3443553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Del (9p) syndrome: report of four cases.
    Hou JW
    Acta Paediatr Taiwan; 2003; 44(1):50-3. PubMed ID: 12800387
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S; del Rey G; Heinrich J; Coco R
    Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pure trisomy 19p syndrome in an infant with an extra ring chromosome.
    Novelli A; Ceccarini C; Bernardini L; Zuccarello D; Digilio MC; Mingarelli R; Dallapiccola B
    Cytogenet Genome Res; 2005; 111(2):182-5. PubMed ID: 16103663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
    Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU; Baumann WA
    Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.