BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 3561951)

  • 1. Retinal cone dysfunction and mental retardation associated with a de novo balanced translocation 1;6(q44;q27).
    Tranebjaerg L; Sjø O; Warburg M
    Ophthalmic Paediatr Genet; 1986 Dec; 7(3):167-73. PubMed ID: 3561951
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardation.
    Neetha J; Girisha KM; Gopinath PM; Sekhar MR
    Genet Couns; 2012; 23(4):473-6. PubMed ID: 23431746
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Retinal cone dystrophy and chromosome 6(q26) deletions.
    Warburg M; Tranebjaerg L; Sjö O
    Ann Genet; 1990; 33(2):124. PubMed ID: 2241088
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease.
    Lamb J; Wilkie AO; Harris PC; Buckle VJ; Lindenbaum RH; Barton NJ; Reeders ST; Weatherall DJ; Higgs DR
    Lancet; 1989 Oct; 2(8667):819-24. PubMed ID: 2477654
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A, 1;6, translocation associated with congenital glaucoma and cleft lip and palate.
    Tinning S; Jacobsen P; Mikkelsen M
    Hum Hered; 1975; 25(6):453-60. PubMed ID: 1225819
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial trisomy 2p.
    Pueschel SM; Scola PS; Mendoza T
    J Ment Defic Res; 1987 Sep; 31 ( Pt 3)():293-8. PubMed ID: 3681957
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Complex chromosome rearrangement involving chromosomes 1, 4 and 16 revealed by fluorescence in situ hybridization.
    Johannesson T; Ehlers S; Wahlström J
    Clin Genet; 1997 Apr; 51(4):281-5. PubMed ID: 9184255
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype.
    Evans K; Duvall-Young J; Fitzke FW; Arden GB; Bhattacharya SS; Bird AC
    Arch Ophthalmol; 1995 Feb; 113(2):195-201. PubMed ID: 7864751
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cytogenetic and molecular characterization of a patient with partial 6q trisomy and 1q monosomy].
    Qin F; Lu X; Feng Y; Tang P; Niu G; Li F; Zhang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):231-4. PubMed ID: 27060323
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complex translocation in a boy with trichorhinophalangeal syndrome.
    Sánchez LM; Labarta JD; De Negrotti TC; Migliorini AM
    J Med Genet; 1985 Aug; 22(4):314-6. PubMed ID: 4045963
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).
    D'Alessandro E; Ligas C; Lo Re ML; Marcanio MP; Gentile T; Del Porto G
    J Med Genet; 1994 May; 31(5):413-5. PubMed ID: 8064823
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of a de novo complex chromosomal rearrangement involving four chromosomes.
    Kim HJ; Perle MA; Bogosian V; Greco A
    Prenat Diagn; 1986; 6(3):211-6. PubMed ID: 3725740
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature.
    Perrone MD; Rocca MS; Bruno I; Faletra F; Pecile V; Gasparini P
    Eur J Med Genet; 2012 Feb; 55(2):117-9. PubMed ID: 22186213
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy 9p with i(9p) and t(9q18p).
    Herva R; Koivisto M
    Hum Genet; 1979 Sep; 50(3):237-40. PubMed ID: 489006
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 1q42-qter associated with monosomy 6q27-qter: a case report.
    Tartaglia E; Mastrantonio P; Costa D; Giugliano B; Porcellini A; Costagliola C
    Eur J Ophthalmol; 2011; 21(3):315-9. PubMed ID: 20954143
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities].
    Gregori Romero M; Gil Benso R; López Ginés C; Pellín Pérez A; Barberá Guillem E
    An Esp Pediatr; 1984 Oct; 21(6):593-6. PubMed ID: 6524770
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Williams syndrome and chromosome 18.
    Menko FH; Stouthart PJ
    J Med Genet; 1992 Sep; 29(9):679-80. PubMed ID: 1404306
    [No Abstract]   [Full Text] [Related]  

  • 19. De novo direct duplication 3 (p25-->pter): a previously undescribed chromosomal aberration.
    Kotzot D; Krüger C; Braun-Quentin C
    Clin Genet; 1996 Aug; 50(2):96-8. PubMed ID: 8937769
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Balanced translocations in mental retardation.
    Vandeweyer G; Kooy RF
    Hum Genet; 2009 Jul; 126(1):133-47. PubMed ID: 19347365
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.