BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 20449811)

  • 1. Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome.
    Burégio-Frota P; Valença L; Leal GF; Duarte AR; Bispo-Brito AV; Soares-Ventura EM; Marques-Salles TJ; Nogueira MT; Muniz MT; Silva ML; Hunstig F; Liehr T; Santos N
    Genet Mol Res; 2010 Apr; 9(2):780-4. PubMed ID: 20449811
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo duplication xq22-q23 in a girl with short stature and gonadal dysgenesis.
    Correa-Cerro L; Garcia-Cruz D; Ruiz MX; Sanchez-Corona J
    Ann Genet; 1999; 42(1):41-4. PubMed ID: 10214506
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytogenetic evaluation, fluorescence in situ hybridization, and molecular study of psu idic(X)(pter-->q22.3::q22.3-->pter) chromosome abberation in a girl with moderate growth retardation.
    Petković I; Barisić I; Bago R
    Croat Med J; 2003 Aug; 44(4):494-9. PubMed ID: 12950157
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
    Wolff DJ; Schwartz MF; Cohen MM; Schwartz S
    Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
    Canún S; Mutchinick O; Shaffer LG; Fernández C
    Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ullrich-Turner syndrome (45,X/46,X,i[Xq]) in a child with a familial inversion of chromosome 3.
    Stine SB; Clark CE; Telfer MA; Casey PA; Cowell HR
    Am J Med Genet; 1982 May; 12(1):57-62. PubMed ID: 7091197
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Pregnancy and the Turner syndrome.
    King CR; Magenis E; Bennett S
    Obstet Gynecol; 1978 Nov; 52(5):617-24. PubMed ID: 724182
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
    Spinner NB; Zackai E; Cheng SD; Knoll JH
    Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A second case of (de novo) paracentric inversion of the short arm of the X chromosome].
    Dahoun S
    Ann Genet; 1990; 33(1):52-5. PubMed ID: 2195983
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unique unbalanced X;X translocation (Xq22;p11.2) in a woman with primary amenorrhea but without Ullrich-Turner syndrome.
    Letterie GS
    Am J Med Genet; 1995 Dec; 59(4):414-6. PubMed ID: 8585557
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome.
    Bergman A; Blennow E
    Eur J Hum Genet; 2000 Oct; 8(10):801-4. PubMed ID: 11039583
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome.
    Gersak K; Writzl K; Veble A; Liehr T
    Genet Couns; 2010; 21(3):335-42. PubMed ID: 20964126
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathy.
    Witters I; Van Buggenhout G; Moerman P; Fryns JP
    Prenat Diagn; 1998 Dec; 18(12):1304-7. PubMed ID: 9885024
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
    Abeliovich D; Dagan J; Lerer I; Silberstein S; Katznelson MB; Frydman M
    Am J Med Genet; 1996 Dec; 66(1):45-51. PubMed ID: 8957510
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure.
    Chen CP; Su YN; Lin HH; Chern SR; Tsai FJ; Wu PC; Lee CC; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):339-44. PubMed ID: 22030050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Turner syndrome. Cytogenetic analysis of 165 patients with Turner syndrome. 1st report].
    Vignetti P; Brinchi V; Bruni L; Rizzuti A; Tarani L; Tozzi MC
    Minerva Pediatr; 1990; 42(1-2):25-7. PubMed ID: 2336052
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.