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 *

107 related articles for article (PubMed ID: 3613245)

  • 21. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
    Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V
    Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376
    [No Abstract]   [Full Text] [Related]  

  • 23. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.
    Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW
    Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature.
    Fryns JP; Kleczkowska A; Van den Berghe H
    Ann Genet; 1990; 33(1):43-5. PubMed ID: 2195980
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Trisomy 4p. A case presentation (author's transl)].
    Delgado A; Egüés J; Muñoz M; González Villa P; Bernaola E; del Amo A
    An Esp Pediatr; 1981 Oct; 15(4):383-9. PubMed ID: 7337304
    [No Abstract]   [Full Text] [Related]  

  • 26. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Partial distal 12q trisomy.
    de Muelenaere A; Fryns JP; Van Den Berghe H
    Ann Genet; 1980; 23(4):251-3. PubMed ID: 6971608
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD; Hansen KL; Littlefield CA
    Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mosaicism for duplication 12q (12q13-->q24.2) in a dysmorphic male infant.
    Dixon JW; Costa T; Teshima IE
    J Med Genet; 1993 Jan; 30(1):70-2. PubMed ID: 8423612
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mosaic isochromosome 12p.
    Pauli RM; Zeier RA; Sekhon GS
    Am J Med Genet; 1987 Jun; 27(2):291-4. PubMed ID: 3605215
    [No Abstract]   [Full Text] [Related]  

  • 32. [Equilibrated 2-14 translocation in a mother and partial trisomy of a pair of the short branches of a number 2 chromosome in 2 of her children].
    Stoll C; Messer J; Vors J
    Ann Genet; 1974 Sep; 17(3):193-6. PubMed ID: 4548821
    [No Abstract]   [Full Text] [Related]  

  • 33. ["De novo" partial trisomy 16p (author's transl)].
    Gabarrón Llamas J; Cabrerizo Portero D; Montserrat Bernal F; Rodríguez Costa T; Cabrerizo Merino C; Rodríguez López F
    An Esp Pediatr; 1981 Dec; 15(6):587-91. PubMed ID: 7337311
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)].
    Menéndez I; Casaña H
    Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome.
    Fryns JP; Kleczkowska A; Decock P; Van den Berghe H
    Ann Genet; 1990; 33(1):46-8. PubMed ID: 2195981
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
    Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Psychopathologic symptoms in 2 cases of partial trisomy 13].
    Schröder SG; Wiesbeck GA; Heilbronner H; Täschner KL
    Nervenarzt; 1990 Nov; 61(11):688-91. PubMed ID: 2290454
    [No Abstract]   [Full Text] [Related]  

  • 38. A de novo tandem duplication 15(q21 leads to qter) mosaic.
    Yip MY; Parsons A; Hultén M
    Clin Genet; 1982 Jul; 22(1):1-6. PubMed ID: 7172470
    [No Abstract]   [Full Text] [Related]  

  • 39. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
    Oliveira-Duarte MH; Martelli-Soares LR; Sarquis-Cintra T; Machado ML; Lison MP
    Ann Genet; 1990; 33(1):56-9. PubMed ID: 2195984
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A
    An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.