BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 11102935)

  • 1. Unbalanced 4;6 translocation and progressive renal disease.
    Pierpont ME; Hentges AS; Gears LJ; Hirsch B; Sinaiko A
    Am J Med Genet; 2000 Nov; 95(3):275-80. PubMed ID: 11102935
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.
    Senses DA; Silan F; Uzun H; Alagöz D; Zafer C; Kocabay K; Karaüzüm SB; Cetin Z
    Genet Couns; 2007; 18(2):163-70. PubMed ID: 17710868
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
    Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
    Brisset S; Joly G; Ozilou C; Lapierre JM; Gosset P; LeLorc'h M; Raoul O; Turleau C; Vekemans M; Romana SP
    Am J Med Genet; 2002 Dec; 113(4):339-45. PubMed ID: 12457405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. "Essentially pure" partial trisomy (6)(p23-->pter) in two brothers due to maternal t(6;17)(p23;p13.3).
    Röthlisberger B; Kotzot D; Gnehm HE; Schinzel A
    Am J Med Genet; 1999 Aug; 85(4):389-94. PubMed ID: 10398266
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [4p trisomy secondary to paternal translocation t(4p-;15q+)].
    Saad A; Khelif M; Kharrat H; Bouzakoura C
    Ann Pediatr (Paris); 1991 May; 38(5):350-4. PubMed ID: 1872531
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M; Hemly NA; Zaki MS
    Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
    Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
    Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
    Rudnik-Schöneborn S; Schubert R; Majewski F; Haverkamp F; Schwanitz G
    Clin Genet; 1997 Aug; 52(2):126-9. PubMed ID: 9298749
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
    Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
    Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
    Sebastio G; Perone L; Guzzetta V; Sebastio L; Vicari L; Della Casa R; Gurrieri F; Zappata S; Pomponi MG; Mazzei A; Neri G; Andria G; Brahe C
    Am J Med Genet; 1996 May; 63(2):366-72. PubMed ID: 8725787
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes.
    Byatt SA; Baker E; Richards RI; Roberts C; Smith A
    Am J Med Genet; 1997 Jun; 70(4):357-60. PubMed ID: 9182774
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Terminal deletion of 6p: report of a new case.
    Plaja A; Vidal R; Soriano D; Bou X; Vendrell T; Mediano C; Pueyo JM; Labraña X; Sarret E
    Ann Genet; 1994; 37(4):196-9. PubMed ID: 7710255
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?
    Breuning MH; Bijlsma JB; de France HF
    Hum Genet; 1977 Aug; 38(1):7-13. PubMed ID: 903156
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Familial 4;18 chromosome translocation resulting in trisomy 4p and monosomy 18p: affected individuals with discordant phenotype.
    Berman DR; Couyoumjian CA; Treadwell MC; Barr M
    Prenat Diagn; 2009 May; 29(5):538-40. PubMed ID: 19226522
    [No Abstract]   [Full Text] [Related]  

  • 17. Trisomy 17p11-pter: unbalanced pericentric inversion, inv(17)(p11q25) in two patients, unbalanced translocations t(4;17)(q27;p11) in a newborn and t(4;17) (p16;p11.2) in a fetus.
    Lurie IW; Gurevich DB; Binkert F; Schinzel A
    Clin Dysmorphol; 1995 Jan; 4(1):25-32. PubMed ID: 7735502
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
    Casaccia G; Mobili L; Braguglia A; Santoro F; Bagolan P
    Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial trisomy of long arm of chromosome 4 as a result of dir dup (4)(q27q31.3) de novo.
    Hubert E; Sawicka A; Wasilewska E; Midro AT
    Genet Couns; 2006; 17(2):211-8. PubMed ID: 16970040
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.