BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 11471169)

  • 21. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
    Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
    Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
    Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
    [TBL] [Abstract][Full Text] [Related]  

  • 23. De novo t(5p;21q) in a patient previously diagnosed as monosomy 21.
    López-Pajares I; Martin-Ancel A; Cabello P; Delicado A; Garcia-Alix A; San Roman C
    Clin Genet; 1993 Feb; 43(2):94-7. PubMed ID: 8448910
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting.
    Abuelo DN; Ahsanuddin AN; Mark HF
    Am J Med Genet; 2000 Oct; 94(5):392-9. PubMed ID: 11050625
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
    McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
    Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB; Stevens CA
    Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Partial monosomy 21 (q11.2→q21.3) combined with 3p25.3→pter monosomy due to an unbalanced translocation in a patient presenting dysmorphic features and developmental delay.
    dos Santos AP; Vieira TP; Simioni M; Monteiro FP; Gil-da-Silva-Lopes VL
    Gene; 2013 Jan; 513(2):301-4. PubMed ID: 23031812
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH; Cho HS; Lee ES; Jung BC
    Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Interstitial deletion of the long arm of chromosome 5 in a boy with multiple congenital anomalies and mental retardation: Molecular characterization of the deleted region to 5q22.3q23.3.
    Garcia-Miñaur S; Ramsay J; Grace E; Minns RA; Myles LM; FitzPatrick DR
    Am J Med Genet A; 2005 Feb; 132A(4):402-10. PubMed ID: 15742475
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T; van den Berghe L; Smeets E; Fryns JP
    Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Deletion 2p15-16.1 syndrome: case report and review.
    Prontera P; Bernardini L; Stangoni G; Capalbo A; Rogaia D; Romani R; Ardisia C; Dallapiccola B; Donti E
    Am J Med Genet A; 2011 Oct; 155A(10):2473-8. PubMed ID: 21910216
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
    Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
    Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome.
    Filges I; Röthlisberger B; Boesch N; Weber P; Wenzel F; Huber AR; Heinimann K; Miny P
    Am J Med Genet A; 2010 Apr; 152A(4):987-93. PubMed ID: 20358614
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
    Blennow E; Bui TH; Wallin A; Kogner P
    Am J Med Genet; 1996 Oct; 65(1):60-7. PubMed ID: 8914743
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Abnormalities of chromosome 22 in meningiomas and confirmation of the origin of a dicentric 22 by in situ hybridization.
    Tonk V; Osella P; Delasmorenas A; Wyandt HE; Milunsky A
    Cancer Genet Cytogenet; 1992 Nov; 64(1):65-8. PubMed ID: 1458452
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
    J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
    [TBL] [Abstract][Full Text] [Related]  

  • 37. De novo interstitial deletion of chromosome 1p with absent corpus callosum--a case report.
    Sivasankaran S; Ho NK; Knight L
    Ann Acad Med Singap; 1997 Jul; 26(4):507-9. PubMed ID: 9395821
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter.
    Fan YS; Siu VM
    Am J Med Genet; 2001 Aug; 102(3):266-71. PubMed ID: 11484205
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A supernumerary marker chromosome with a neocentromere derived from 5p14-->pter.
    Fritz B; Dietze I; Wandall A; Aslan M; Schmidt A; Kattner E; Schwerdtfeger R; Friedrich U
    J Med Genet; 2001 Aug; 38(8):559-65. PubMed ID: 11494970
    [No Abstract]   [Full Text] [Related]  

  • 40. Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia.
    Tsao CY; Wenger GD; Bartholomew DW
    Am J Med Genet A; 2005 Apr; 134A(2):198-201. PubMed ID: 15690344
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.