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 *

146 related articles for article (PubMed ID: 9643298)

  • 1. Three patients with a 45,X/46,X,psu dic(Xp) karyotype.
    Dalton P; Coppin B; James R; Skuse D; Jacobs P
    J Med Genet; 1998 Jun; 35(6):519-24. PubMed ID: 9643298
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.
    Callen DF; Mulley JC; Baker EG; Sutherland GR
    Hum Genet; 1987 Nov; 77(3):236-40. PubMed ID: 3479386
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Two dicentric Y isochromosomes, one without and the Yqh heterochromatic segment: review of the Y isochromosomes.
    Daniel A; Lyons N; Casey JH; Gras L
    Hum Genet; 1980; 54(1):31-9. PubMed ID: 7190126
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [X isochromosomes: delayed diagnosis of Turner's syndrome].
    Cuesta Hernández M; Rueda Valencia ME; Pérez Rodríguez O; López de Lara D
    An Pediatr (Barc); 2015 Jan; 82(1):e131-4. PubMed ID: 25475905
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes.
    Cooper C; Crolla JA; Laister C; Johnston DI; Cooke P
    J Med Genet; 1991 Jan; 28(1):6-9. PubMed ID: 1999837
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Single-nucleotide polymorphism array genotyping is equivalent to metaphase cytogenetics for diagnosis of Turner syndrome.
    Prakash S; Guo D; Maslen CL; Silberbach M; Milewicz D; Bondy CA;
    Genet Med; 2014 Jan; 16(1):53-9. PubMed ID: 23743550
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Study of isochromosomes of the long arms of the X chromosome].
    Borrego S; Fernández-Novoa C; San Martín V; Novales A; Hevia A; Galera H
    An Esp Pediatr; 1988 Aug; 29(2):117-21. PubMed ID: 3190016
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes.
    Monroy N; López M; Cervantes A; García-Cruz D; Zafra G; Canún S; Zenteno JC; Kofman-Alfaro S
    Am J Med Genet; 2002 Jan; 107(3):181-9. PubMed ID: 11807897
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic investigation of six patients with X isochromosomes, i(Xq), and of two subjects with isodicentric X chromosomes, idic (Xq).
    Gaál M; László J; Bösze P
    Hum Genet; 1981; 58(4):362-5. PubMed ID: 7327558
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies.
    Shankman S; Spurdle AB; Morris D; Rosendorff J; Marques I; Bernstein R; Ramsay M
    Am J Med Genet; 1995 Jan; 55(3):269-75. PubMed ID: 7726221
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Sex chromosome aberrations in patients with menstruation disorders].
    Midro AT; Panasiuk B; Radwan J; Sipowicz I; Jaworowska B; Korsak E
    J Gynecol Obstet Biol Reprod (Paris); 1990; 19(7):811-6. PubMed ID: 2277162
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
    Wolff DJ; Miller AP; Van Dyke DL; Schwartz S; Willard HF
    Am J Hum Genet; 1996 Jan; 58(1):154-60. PubMed ID: 8554051
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Turner syndrome isochromosome karyotype correlates with decreased dental crown width.
    Rizell S; Barrenäs ML; Andlin-Sobocki A; Stecksén-Blicks C; Kjellberg H
    Eur J Orthod; 2012 Apr; 34(2):213-8. PubMed ID: 21303812
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system.
    Higgins AW; Schueler MG; Willard HF
    Chromosoma; 1999 Aug; 108(4):256-65. PubMed ID: 10460414
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndrome.
    Robinson DO; Dalton P; Jacobs PA; Mosse K; Power MM; Skuse DH; Crolla JA
    J Med Genet; 1999 Apr; 36(4):279-84. PubMed ID: 10227393
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.
    Tsezou A; Hadjiathanasiou C; Gourgiotis D; Galla A; Kavazarakis E; Pasparaki A; Kapsetaki M; Sismani C; Theodoridis C; Patsalis PC; Moschonas N; Kitsiou S
    Clin Genet; 1999 Dec; 56(6):441-6. PubMed ID: 10665663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].
    Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity.
    Sharp CB; Bedford HM; Willard HF
    Hum Genet; 1990 Aug; 85(3):330-6. PubMed ID: 2394446
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.