BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 1781959)

  • 1. A case with laryngeal atresia and partial trisomy 9 due to maternal 9;16 translocation.
    Van den Boogaard MJ; De Pater J; Hennekam RC
    Genet Couns; 1991; 2(2):83-91. PubMed ID: 1781959
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Syndrome of congenital malformations and dysmorphic features in a newborn with partial trisomy 16q due to maternal translocation t(9;16)(p24;q13)].
    Luberda-Zapaśnik J; Midro AT; Szwałkiewicz-Warowicka E
    Pediatr Pol; 1995 Sep; 70(9):769-73. PubMed ID: 8657511
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
    Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
    Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
    Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy 9q due to maternal 9q 17q translocation.
    Nampoothiri S; Lakshman LR; Anilkumar A; Thampi MV
    Indian Pediatr; 2008 Jul; 45(7):595-8. PubMed ID: 18695283
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular studies of translocations and trisomy involving chromosome 13.
    Robinson WP; Bernasconi F; Dutly F; Lefort G; Romain DR; Binkert F; Schinzel AA
    Am J Med Genet; 1996 Jan; 61(2):158-63. PubMed ID: 8669444
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
    Siffroi JP; Romani F; Viguié F; Lejeune C
    Ann Genet; 1984; 27(4):241-4. PubMed ID: 6335372
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 17q and monosomy 9p due to a familial translocation.
    Cotter PD; Stewart NL
    Ann Genet; 1990; 33(4):231-3. PubMed ID: 1710432
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A rare combination of partial trisomy 9 with pulmonary atresia].
    Nekarda T; Kececioglu D; Kehl HG; Gehrmann J; Miny P; Vogt J
    Klin Padiatr; 1997; 209(3):127-9. PubMed ID: 9244820
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 16q resulting from maternal translocation 11p/16q.
    Calva P; Frias S; Carnevale A; Reyes P
    Ann Genet; 1984; 27(2):122-5. PubMed ID: 6331790
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberration.
    Eggermann T; Kolin-Gerresheim I; Gerresheim F; Schwanitz G
    Ann Genet; 1998; 41(4):205-8. PubMed ID: 9881183
    [TBL] [Abstract][Full Text] [Related]  

  • 13. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
    Abeliovich D; Dagan J; Lerer I; Silberstein S; Katznelson MB; Frydman M
    Am J Med Genet; 1996 Dec; 66(1):45-51. PubMed ID: 8957510
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)].
    Rethoré MO; Lafourcade J; Couturier J; Harpey JP; Hamet M; Engler R; Alcindor LG; Lejeune J
    Ann Genet; 1982; 25(1):36-42. PubMed ID: 6979298
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T; Acar H; Oran B
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. [16q+ partial trisomy in a 7-day-old surviving neonate].
    Zidovská J; Bobeková A; Stloukalová M; Svarcová M
    Cesk Pediatr; 1989 Oct; 44(10):608-9. PubMed ID: 2620355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter.
    Yamada K; Uchiyama A; Arai M; Kubodera K; Yamamoto Y; Orii KO; Nagasawa H; Masuno M; Kohno Y
    Congenit Anom (Kyoto); 2009 Jun; 49(2):85-8. PubMed ID: 19489960
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Combined trisomy 9P and Shprintzen syndrome resulting from a paternal t(9;22).
    Komatsu H; Kihara A; Komura E; Mitsufuji N; Tsujii H; Kakita S; Ikuta H
    Genet Couns; 2001; 12(2):137-43. PubMed ID: 11491308
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
    D'Emma C; Crippa L; Delozier C; Michail E; Graber P
    J Genet Hum; 1982 Mar; 30(1):39-50. PubMed ID: 7130955
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.