BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 7604850)

  • 1. Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).
    Scheuerle A; Zenger-Hain JL; Van Dyke DL; Ledbetter DH; Greenberg F; Shaffer LG
    Am J Med Genet; 1995 May; 56(4):403-8. PubMed ID: 7604850
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cri du chat and Turner syndrome features in a newborn girl with an unbalanced 45,X,psu dic(5;X)(p15.2;p22.1) karyotype: FISH and replication banding studies.
    Reddy KS; Smith DL; Ball CS
    Ann Genet; 1999; 42(2):105-8. PubMed ID: 10434125
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
    Klein OD; Cotter PD; Albertson DG; Pinkel D; Tidyman WE; Moore MW; Rauen KA
    Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
    [TBL] [Abstract][Full Text] [Related]  

  • 4. True telomeric translocation in a baby with the Prader-Willi phenotype.
    Reeve A; Norman A; Sinclair P; Whittington-Smith R; Hamey Y; Donnai D; Read A
    Am J Med Genet; 1993 Aug; 47(1):1-6. PubMed ID: 8368237
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
    Kousseff BG; Diamond T; Essig Y; Miller K; Tedesco T
    Am J Med Genet; 1987 Dec; 28(4):803-11. PubMed ID: 3688018
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
    Pettenati MJ; Teot LA; Smith C; Hayworth R; Thomas IT; Veille JC; Rao PN
    Am J Med Genet; 1993 Feb; 45(3):365-9. PubMed ID: 8434625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.
    Williams CA; Gray BA; Hendrickson JE; Stone JW; CantĂș ES
    Am J Med Genet; 1989 Mar; 32(3):339-45. PubMed ID: 2786338
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
    Cole H; Huang B; Salbert BA; Brown J; Howard-Peebles PN; Black SH; Dorfmann A; Febles OR; Stevens CA; Jackson-Cook C
    Am J Med Genet; 1994 Aug; 52(2):136-45. PubMed ID: 7801998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
    Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
    Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Y/15 translocation in a 45,X male with Prader-Willi syndrome.
    Puvabanditsin S; Garrow E; Razi S; Mohar AG; Tadros JJ; Phattraprayoon N; Patel P
    Genet Couns; 2007; 18(4):417-21. PubMed ID: 18286823
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
    Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
    Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation.
    Sharp A; Robinson DO; Jacobs P
    Hum Genet; 2001 Sep; 109(3):295-302. PubMed ID: 11702210
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lack of X inactivation: loss of one X inactivation center in a case with mos45,X,-21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2).
    Ishikiriyama S; Iai M; Tanabe Y
    Am J Med Genet; 1993 Aug; 47(1):41-4. PubMed ID: 8368250
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).
    Park JP; Moeschler JB; Hani VH; Hawk AB; Belloni DR; Noll WW; Mohandas TK
    Am J Med Genet; 1998 Jun; 78(2):134-9. PubMed ID: 9674903
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 46,X,i(Xq)/47,XX,+13 mosaicism.
    Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T
    Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-inactivation pattern in three cases of X/autosome translocation.
    Zabel BU; Baumann WA; Pirntke W; Gerhard-Ratschow K
    Am J Med Genet; 1978; 1(3):309-17. PubMed ID: 677170
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
    Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
    Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exclusion of uniparental inheritance of chromosome 15 in a fetus with a familial dicentric (Y;15) translocation.
    White LM; Treat K; Leff A; Styers D; Mitchell M; Knoll JH
    Prenat Diagn; 1998 Feb; 18(2):111-6. PubMed ID: 9516010
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mosaicism with a normal cell line and an unbalanced structural rearrangement.
    Zaslav AL; Fallet S; Blumenthal D; Jacob J; Fox J
    Am J Med Genet; 1999 Jan; 82(1):15-9. PubMed ID: 9916836
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.