These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


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.