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 *

103 related articles for article (PubMed ID: 9179806)

  • 1. Molecular and cytogenetic studies of X inactivation in a patient with 46,X,del(X)(q22).
    Witchel SF; Wenger SL; Hoffman EP
    J Pediatr Adolesc Gynecol; 1997 May; 10(2):78-82. PubMed ID: 9179806
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Del Xq23 in a mosaic Turner female: molecular and cytogenetic studies.
    Mesa-Cornejo VM; García-Cruz D; Monroy-Jaramillo N; Vásquez AI; Dávalos NO; Galaviz C; Kofman S
    Ann Genet; 2001; 44(4):171-4. PubMed ID: 11755099
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A study of females with deletions of the short arm of the X chromosome.
    James RS; Coppin B; Dalton P; Dennis NR; Mitchell C; Sharp AJ; Skuse DH; Thomas NS; Jacobs PA
    Hum Genet; 1998 May; 102(5):507-16. PubMed ID: 9654198
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.
    Callen DF; Eyre HJ; Dolman G; Garry-Battersby MB; McCreanor JR; Valeba A; McGill JJ
    J Med Genet; 1995 Feb; 32(2):113-6. PubMed ID: 7760319
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gonadal and statural determinants on the X chromosome and their relationship to in vitro studies showing prolonged cell cycles in 45,X; 46,X,del(X)(p11); 46,X,del(X)(q13); and 46,X,del(X)(q22) fibroblasts.
    Simpson JL; Lebeau MM
    Am J Obstet Gynecol; 1981 Dec; 141(8):930-40. PubMed ID: 7315923
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features.
    Adachi M; Tachibana K; Asakura Y; Muroya K; Ogata T
    Hum Genet; 2000 Mar; 106(3):306-10. PubMed ID: 10798359
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea.
    Ruthner U; Maschik S; Friedrich F; Breitenecker G
    Hum Genet; 1979 Apr; 48(1):135-7. PubMed ID: 457129
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Turner syndrome-associated neurocognitive phenotype maps to distal Xp.
    Ross JL; Roeltgen D; Kushner H; Wei F; Zinn AR
    Am J Hum Genet; 2000 Sep; 67(3):672-81. PubMed ID: 10931762
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular and cytogenetic analysis of familial Xp deletions.
    Wandstrat AE; Conroy JM; Zurcher VL; Pasztor LM; Clark BA; Zackowski JL; Schwartz S
    Am J Med Genet; 2000 Sep; 94(2):163-9. PubMed ID: 10982973
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location.
    Boucher CA; Sargent CA; Ogata T; Affara NA
    J Med Genet; 2001 Sep; 38(9):591-8. PubMed ID: 11546827
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center.
    Pettigrew AL; McCabe ER; Elder FF; Ledbetter DH
    Hum Genet; 1991 Aug; 87(4):498-502. PubMed ID: 1879836
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial short arm deletions of the X chromosome and spontaneous pubertal development in girls with short stature.
    Kalousek D; Schiffrin A; Berguer AM; Spier P; Guyda H; Colle E
    J Pediatr; 1979 Jun; 94(6):891-4. PubMed ID: 448530
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assessment of X bends in patients with atypical X chromosome phenotypes.
    Munn CA; Wenger SL; Steele MW
    Ann Genet; 1991; 34(2):120-4. PubMed ID: 1746882
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes.
    Yorifuji T; Muroi J; Kawai M; Uematsu A; Sasaki H; Momoi T; Kaji M; Yamanaka C; Furusho K
    J Med Genet; 1998 Jul; 35(7):539-44. PubMed ID: 9678697
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients.
    Ogata T; Muroya K; Matsuo N; Shinohara O; Yorifuji T; Nishi Y; Hasegawa Y; Horikawa R; Tachibana K
    J Clin Endocrinol Metab; 2001 Nov; 86(11):5498-508. PubMed ID: 11701728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Gonadal function in Turner syndrome].
    Alves M; Bastos M; Almeida Santos T; Carrilho F
    Acta Med Port; 2013; 26(6):655-63. PubMed ID: 24388251
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Del (X)(p21.2) in a mother and two daughters with variable ovarian function.
    Zinn AR; Ouyang B; Ross JL; Varma S; Bourgeois M; Tonk V
    Clin Genet; 1997 Oct; 52(4):235-9. PubMed ID: 9383030
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Random X inactivation in a girl with a balanced t(X;9) and an abnormal phenotype.
    Wolff DJ; Schwartz S; Montgomery T; Zackowski JL
    Am J Med Genet; 1998 Jun; 77(5):401-4. PubMed ID: 9632170
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.
    Chen CP; Kuo YK; Su YN; Chern SR; Tsai FJ; Wu PC; Chen YT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.