BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

614 related articles for article (PubMed ID: 7856666)

  • 1. 18q- and 18q+ mosaicism in a mentally retarded boy.
    Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
    Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Chromosomal mosaicism in the r (15) syndrome].
    Malygina NA; Mutovin GR; Filina NP; Akif'ev AP
    Genetika; 1980; 16(11):2029-33. PubMed ID: 7193157
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
    Syrrou M; Borghgraef M; Fryns JP
    Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R; Paolieri M; Anichini C; Scarinci R; Berardi R; Rosaia L; Pucci L
    Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
    Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
    Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
    [No Abstract]   [Full Text] [Related]  

  • 6. Isochromosome-formation in chromosome 9.
    Miller K; Arslan-Kirchner M
    Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.
    Juyal RC; Kuwano A; Kondo I; Zara F; Baldini A; Patel PI
    Am J Med Genet; 1996 Dec; 66(2):193-6. PubMed ID: 8958329
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype.
    Speevak M; Hunter AG; Hughes H; Cox DM
    Ann Genet; 1985; 28(3):177-80. PubMed ID: 3879153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG; Towner JW; Forsman I; Siris E
    Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndrome.
    Urioste M; Visedo G; Sanchís A; Sentís C; Villa A; Ludeña P; Hortigüela JL; Martínez-Frías ML; Fernández-Piqueras J
    Am J Med Genet; 1994 Jan; 49(1):77-82. PubMed ID: 8172255
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 46,XY del(18)(q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome.
    Maaswinkel-Mooij PD; de Jong P; Beverstock GC
    Clin Genet; 1993 Feb; 43(2):76-8. PubMed ID: 8448905
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
    Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletion of the band 4p15.3 defined by sequential replication banding.
    Davies J; Voullaire L; Bankier A
    Ann Genet; 1990; 33(2):92-5. PubMed ID: 2241091
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization.
    Mewar R; Kline AD; Jackson L; Overhauser J
    Am J Med Genet; 1992 Nov; 44(4):477-81. PubMed ID: 1442891
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mosaic supernumerary small ring chromosome.
    Fryns JP; van Herck G; van den Berghe H
    J Genet Hum; 1981 Jun; 29(2):151-4. PubMed ID: 7328409
    [No Abstract]   [Full Text] [Related]  

  • 17. Long arm deletion of chromosome no. 6 in a mentally retarded boy with multiple physical malformations.
    Milosević J; Kalicanin P
    J Ment Defic Res; 1975 Jun; 19(2):139-44. PubMed ID: 1195357
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
    Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rieger syndrome and interstitial 4q26 deletion.
    Fryns JP; Van Den Berghe H
    Genet Couns; 1992; 3(3):153-4. PubMed ID: 1388934
    [No Abstract]   [Full Text] [Related]  

  • 20. Mosaic isochromosome 8p.
    Tilstra DJ; Grove M; Spencer AC; Norwood TH; Pagon RA
    Am J Med Genet; 1993 Jun; 46(5):517-9. PubMed ID: 8322812
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.