BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 739260)

  • 1. Inherited parital duplication deficiency of chromosome 15 (p12;q22).
    Coco R; Penchaszadeh VB
    J Genet Hum; 1978 Sep; 26(3):203-10. PubMed ID: 739260
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
    Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
    Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS; Summitt RL; Martens P; Gooch WM
    Ann Genet; 1977 Dec; 20(4):237-42. PubMed ID: 305749
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy for the distal part of the long arm of chromosome 15--a new syndrome?
    Kaneko K; Katabuchi H; Maruta H
    Nihon Sanka Fujinka Gakkai Zasshi; 1986 Jun; 38(6):940-4. PubMed ID: 3734522
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The trisomy 4p syndrome: case report and review.
    Gonzalez CH; Sommer A; Meisner LF; Elejalde BR; Opitz JM
    Am J Med Genet; 1977; 1(2):137-56. PubMed ID: 416713
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM; Ornoy A; Rosenmann A; Kohn G
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy of the short arm of chromosome 4: the changing phenotype with age.
    Kleczkowska A; Fryns JP; van den Berghe H
    Ann Genet; 1992; 35(4):217-23. PubMed ID: 1296518
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The 18p- syndrome. Report of five cases.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ["Free" 9p trisomy in a male child with severe mental retardation (author's transl)].
    Aller V; Abrisqueta JA; Martín-Lucas MA; de Torres ML; del Mazo J; Pérez-Castillo A
    An Esp Pediatr; 1979 May; 12(5):463-8. PubMed ID: 464416
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspring.
    Tuck-Muller CM; Varela M; Li S; Pridjian G; Chen H; Wertelecki W
    Am J Med Genet; 1996 May; 63(2):392-5. PubMed ID: 8725792
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocation.
    Chase TR; Jalal SM; Martsolf JT; Wasdahl WA
    Am J Med Genet; 1983 Feb; 14(2):347-51. PubMed ID: 6837629
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
    Cappon SL; Duncan AM; Khalifa MM
    Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
    Gonzalez CH; Billerbeck AE; Takayama LC; Wajntal A
    Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
    Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Proximal trisomy 19q. Interstitial deletion and ring chromosome derived from 19q].
    Klein F; Schuck D; Noël B; Stoessel J; Vibert M
    Pediatrie; 1989; 44(9):717-20. PubMed ID: 2622712
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A patient with 13q-syndrome with mild mental retardation and with growth retardation.
    Stoll C; Alembik Y
    Ann Genet; 1998; 41(4):209-12. PubMed ID: 9881184
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Postaxial polydactyly: a symptom of partial trisomy of the long arm of chromosome 13. Two new observations with 46, XX, t (22;13) (q13;q31) and 46, XY, Dup (13) (pter-q34::q22-qter) (author's transl)].
    Kessel E; Pfeiffer RA; Baisch C
    Klin Padiatr; 1980 Jan; 192(1):85-90. PubMed ID: 7188997
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial, balanced insertional translocation of chromosome 7 leading to offspring with deletion and duplication of the inserted segment, 7p15 leads to 7p21.
    Miller M; Kaufman G; Reed G; Bilenker R; Schinzel A
    Am J Med Genet; 1979; 4(4):323-32. PubMed ID: 539602
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
    Engelen JJ; de Die-Smulders CE; Dirckx R; Verhoeven WM; Tuinier S; Curfs LM; Hamers AJ
    Am J Med Genet; 2002 Apr; 109(2):149-53. PubMed ID: 11977164
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.