BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 15172006)

  • 1. Genitourinary phenotype in XX patients with distal 9p monosomy.
    Fujimoto Y; Okuyama T; Iijima M; Tanaka T; Horikawa R; Yamada K; Ogata T
    Mol Genet Metab; 2004 Jun; 82(2):173-9. PubMed ID: 15172006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sex-determining gene(s) on distal 9p: clinical and molecular studies in six cases.
    Muroya K; Okuyama T; Goishi K; Ogiso Y; Fukuda S; Kameyama J; Sato H; Suzuki Y; Terasaki H; Gomyo H; Wakui K; Fukushima Y; Ogata T
    J Clin Endocrinol Metab; 2000 Sep; 85(9):3094-100. PubMed ID: 10999792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Female gonadal development in XX patients with distal 9p monosomy.
    Ogata T; Muroya K; Ohashi H; Mochizuki H; Hasegawa T; Kaji M
    Eur J Endocrinol; 2001 Nov; 145(5):613-7. PubMed ID: 11720880
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development.
    Ounap K; Uibo O; Zordania R; Kiho L; Ilus T; Oiglane-Shlik E; Bartsch O
    Am J Med Genet A; 2004 Nov; 130A(4):415-23. PubMed ID: 15481033
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p.
    Ogata T; Muroya K; Matsuo N; Hata J; Fukushima Y; Suzuki Y
    J Med Genet; 1997 Apr; 34(4):331-4. PubMed ID: 9138160
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
    Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
    Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H
    Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
    Chen CP; Lin SP; Lee CC; Town DD; Wang W
    Genet Couns; 2006; 17(3):301-6. PubMed ID: 17100198
    [TBL] [Abstract][Full Text] [Related]  

  • 10. M-FISH applications in clinical genetics.
    Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
    Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
    [TBL] [Abstract][Full Text] [Related]  

  • 11. XY sex reversal and gonadal dysgenesis due to 9p24 monosomy.
    McDonald MT; Flejter W; Sheldon S; Putzi MJ; Gorski JL
    Am J Med Genet; 1997 Dec; 73(3):321-6. PubMed ID: 9415692
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
    Petty EM; Gibson LH; Breg WR; Burns JP; Yang-Feng TL
    Am J Med Genet; 1993 Mar; 45(6):770-3. PubMed ID: 8456860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1.
    Veitia R; Nunes M; Brauner R; Doco-Fenzy M; Joanny-Flinois O; Jaubert F; Lortat-Jacob S; Fellous M; McElreavey K
    Genomics; 1997 Apr; 41(2):271-4. PubMed ID: 9143505
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 9p partial monosomy and disorders of sex development: review and postulation of a pathogenetic mechanism.
    Quinonez SC; Park JM; Rabah R; Owens KM; Yashar BM; Glover TW; Keegan CE
    Am J Med Genet A; 2013 Aug; 161A(8):1882-96. PubMed ID: 23824832
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
    Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
    Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
    Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
    Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical, molecular and cytogenetic studies on 4 patients with 46, XX (SRY positive) male syndrome].
    Xia XY; Cui YX; Lu HY; Yang B; Wang GH; Pan LJ; Hou BS; Ge YF; Shao Y; Yao B; Huang YF
    Zhonghua Nan Ke Xue; 2007 Dec; 13(12):1094-7. PubMed ID: 18284058
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses.
    Vialard F; Ottolenghi C; Gonzales M; Choiset A; Girard S; Siffroi JP; McElreavey K; Vibert-Guigue C; Sebaoun M; Joyé N; Portnoï MF; Jaubert F; Fellous M
    J Med Genet; 2002 Jul; 39(7):514-8. PubMed ID: 12114486
    [No Abstract]   [Full Text] [Related]  

  • 19. Mosaic tetrasomy 9p case with the phenotype mimicking Klinefelter syndrome and hyporesponse of gonadotropin-stimulated testosterone production.
    Ogino W; Takeshima Y; Nishiyama A; Yagi M; Oka N; Matsuo M
    Kobe J Med Sci; 2007; 53(4):143-50. PubMed ID: 17932453
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates.
    Shan Z; Zabel B; Trautmann U; Hillig U; Ottolenghi C; Wan Y; Haaf T
    Eur J Hum Genet; 2000 Mar; 8(3):167-73. PubMed ID: 10780781
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.