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 *

134 related articles for article (PubMed ID: 26639996)

  • 1. Chromosome Xq13.2 Microduplication Involving an X-Inactivation Gene in a Girl with Short Stature, Madelung Deformity, and von Willebrand Disease.
    Nur MM; Yamada M; Tonk V; Wilson GN
    J Pediatr Adolesc Gynecol; 2016 Apr; 29(2):e39-42. PubMed ID: 26639996
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Radiological signs of Leri-Weill dyschondrosteosis in Turner syndrome.
    Binder G; Fritsch H; Schweizer R; Ranke MB
    Horm Res; 2001; 55(2):71-6. PubMed ID: 11509862
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spontaneous Sexual Development and Heavy Menstrual Bleeding in 45,X Monosomy and 45,X/47,XXX Mosaic Turner Syndrome and a Review of the Literature.
    Kim MJ; Jeong HR
    J Pediatr Adolesc Gynecol; 2020 Oct; 33(5):602-606. PubMed ID: 32315714
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Turner syndrome and 45,X/47,XXX mosaicism.
    Akbas E; Mutluhan H; Savasoglu K; Soylemez F; Ozturk I; Yazici G
    Genet Couns; 2009; 20(2):141-6. PubMed ID: 19650411
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Epigenetic and transcriptomic consequences of excess X-chromosome material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females.
    Nielsen MM; Trolle C; Vang S; Hornshøj H; Skakkebaek A; Hedegaard J; Nordentoft I; Pedersen JS; Gravholt CH
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):279-293. PubMed ID: 32489015
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [From gene to disease; from SHOX to Lèri-Weill dyschondrosteosis, Turner syndrome and idiopathic short stature].
    Kant SG; Drop SL
    Ned Tijdschr Geneeskd; 2001 Jul; 145(30):1456-9. PubMed ID: 11503314
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unique deletion in exon 5 of SHOX gene in a patient with idiopathic short stature.
    Shanske AL; Puri M; Marshall B; Saenger P
    Horm Res; 2007; 67(2):61-6. PubMed ID: 17028440
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy of the short stature homeobox-containing gene (SHOX) due to duplication/deletion of the X chomosome: clinical implications on the stature.
    Del Rey G; Jasper H; Bengolea SV; Boywitt A; De Bellis R; Heinrich JJ
    Horm Res Paediatr; 2010; 74(4):297-304. PubMed ID: 20689243
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SHOX in short stature syndromes.
    Blaschke RJ; Rappold GA
    Horm Res; 2001; 55 Suppl 1():21-3. PubMed ID: 11408757
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Axenfeld-Rieger spectrum in a patient with 45,X Turner syndrome.
    Abdalla EM; Nabil KM
    Ophthalmic Genet; 2012 Jun; 33(2):111-5. PubMed ID: 22229795
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family.
    Karaman B; Wollnik B; Ermiş H; Yüksel-Apak M; Başaran S
    Prenat Diagn; 2003 Apr; 23(4):336-9. PubMed ID: 12673642
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial Turner syndrome with an X;Y translocation mosaicism: implications for genetic counseling.
    Portnoï MF; Chantot-Bastaraud S; Christin-Maitre S; Carbonne B; Beaujard MP; Keren B; Lévy J; Dommergues M; Cabrol S; Hyon C; Siffroi JP
    Eur J Med Genet; 2012 Nov; 55(11):635-40. PubMed ID: 22809487
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A fertile patient with 45X/47XXX mosaicism.
    Sahinturk S; Ozemri Sag S; Ture M; Gorukmez O; Topak A; Yakut T; Gulten T
    Genet Couns; 2015; 26(1):29-34. PubMed ID: 26043504
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Turner syndrome and schizophrenia: a further hint for the role of the X-chromosome in the pathogenesis of schizophrenic disorders.
    Roser P; Kawohl W
    World J Biol Psychiatry; 2010 Mar; 11(2 Pt 2):239-42. PubMed ID: 20218787
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A unique mosaic Turner syndrome patient with androgen receptor gene derived marker chromosome.
    Kalkan R; Özdağ N; Bundak R; Çirakoğlu A; Serakinci N
    Syst Biol Reprod Med; 2016; 62(1):77-83. PubMed ID: 26744914
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome.
    Ross JL; Kowal K; Quigley CA; Blum WF; Cutler GB; Crowe B; Hovanes K; Elder FF; Zinn AR
    J Pediatr; 2005 Oct; 147(4):499-507. PubMed ID: 16227037
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A Case Report.
    Volejnikova J; Zapletalova J; Jarosova M; Urbankova H; Petr V; Klaskova E; Horwitz MS; Hajduch M; Mihal V
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2018 Mar; 162(1):65-70. PubMed ID: 29469136
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Von Willebrand disease in women with menorrhagia].
    Stefańska E; Vertun-Baranowska B; Windyga J; Łopaciuk S
    Ginekol Pol; 2004 Jan; 75(1):47-52. PubMed ID: 15112473
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A mother with variant Turner syndrome and two daughters with trisomy X: a case report.
    Ramachandram S; Keng WT; Ariffin R; Ganesan V
    J Genet; 2013; 92(2):313-6. PubMed ID: 23970090
    [No Abstract]   [Full Text] [Related]  

  • 20. Girl with partial Turner syndrome and absence epilepsy.
    Puusepp H; Zordania R; Paal M; Bartsch O; Ounap K
    Pediatr Neurol; 2008 Apr; 38(4):289-92. PubMed ID: 18358412
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.