BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

330 related articles for article (PubMed ID: 31070017)

  • 21. Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome.
    Sharma R; Harris VM; Cavett J; Kurien BT; Liu K; Koelsch KA; Fayaaz A; Chaudhari KS; Radfar L; Lewis D; Stone DU; Kaufman CE; Li S; Segal B; Wallace DJ; Weisman MH; Venuturupalli S; Kelly JA; Pons-Estel B; Jonsson R; Lu X; Gottenberg JE; Anaya JM; Cunninghame-Graham DS; Huang AJW; Brennan MT; Hughes P; Alevizos I; Miceli-Richard C; Keystone EC; Bykerk VP; Hirschfield G; Nordmark G; Bucher SM; Eriksson P; Omdal R; Rhodus NL; Rischmueller M; Rohrer M; Wahren-Herlenius M; Witte T; Alarcón-Riquelme M; Mariette X; Lessard CJ; Harley JB; Ng WF; Rasmussen A; Sivils KL; Scofield RH
    Arthritis Rheumatol; 2017 Nov; 69(11):2187-2192. PubMed ID: 28692793
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Acromegaly accompanied by Turner syndrome with 47,XXX/45,X/46,XX mosaicism.
    Yamazaki M; Sato A; Nishio S; Takeda T; Miyamoto T; Katai M; Hashizume K
    Intern Med; 2009; 48(6):447-53. PubMed ID: 19293545
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome.
    Freriks K; Timmers HJ; Netea-Maier RT; Beerendonk CC; Otten BJ; van Alfen-van der Velden JA; Traas MA; Mieloo H; van de Zande GW; Hoefsloot LH; Hermus AR; Smeets DF
    Eur J Med Genet; 2013 Sep; 56(9):497-501. PubMed ID: 23933507
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Serum FSH level below 10 mIU/mL at twelve years old is an index of spontaneous and cyclical menstruation in Turner syndrome.
    Aso K; Koto S; Higuchi A; Ariyasu D; Izawa M; Miyamoto Igaki J; Hasegawa Y
    Endocr J; 2010; 57(10):909-13. PubMed ID: 20798475
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study.
    Berglund A; Viuff MH; Skakkebæk A; Chang S; Stochholm K; Gravholt CH
    Orphanet J Rare Dis; 2019 Jan; 14(1):16. PubMed ID: 30642344
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Turner syndrome phenotype with 47,XXX karyotype: further investigation warranted?
    Wallerstein R; Musen E; McCarrier J; Aisenberg J; Chartoff A; Hutcheon RG; Tepperberg J; Pappenhausen P; Griffin S
    Am J Med Genet A; 2004 Feb; 125A(1):106-7. PubMed ID: 14755478
    [No Abstract]   [Full Text] [Related]  

  • 27. Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome.
    Viuff MH; Stochholm K; Uldbjerg N; Nielsen BB; ; Gravholt CH
    Hum Reprod; 2015 Oct; 30(10):2419-26. PubMed ID: 26251461
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature.
    Butnariu L; Rusu C; Caba L; Pânzaru M; Braha E; Grămescu M; Popescu R; Bujoranu C; Gorduza EV
    Rev Med Chir Soc Med Nat Iasi; 2013; 117(3):714-21. PubMed ID: 24502039
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Atypical Rett syndrome in a girl with mosaic triple X and MECP2 variant.
    Takahashi S; Takeguchi R; Kuroda M; Tanaka R
    Mol Genet Genomic Med; 2020 Mar; 8(3):e1122. PubMed ID: 31943886
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Y chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation case.
    Bispo AV; Burégio-Frota P; Oliveira dos Santos L; Leal GF; Duarte AR; Araújo J; Cavalcante da Silva V; Muniz MT; Liehr T; Santos N
    Reprod Fertil Dev; 2014 Oct; 26(8):1176-82. PubMed ID: 25294360
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. [Application of fluorescence in situ hybridization combined with chromosomal karyotyping analysis in children with disorders of sex development due to sex chromosome abnormalities].
    Wang G; Wang J; Zhang Z; Li R; Li L; Li D; Zhang W; Zhang Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):947-953. PubMed ID: 37532493
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mosaic double aneuploidy (45,X/47,XX,+8) with aortic dissection.
    Lee MN; Choi KH; Kim DK; Kim SH
    Genet Couns; 2014; 25(2):177-82. PubMed ID: 25059016
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: implications for prenatal counseling and estrogen therapy at puberty.
    Blair J; Tolmie J; Hollman AS; Donaldson MD
    J Pediatr; 2001 Nov; 139(5):724-8. PubMed ID: 11713453
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies.
    Massara LS; Delea M; Espeche L; Bruque CD; Oliveri J; Brun P; Furforo L; Dain L; Rozental S
    Cytogenet Genome Res; 2019; 159(3):137-142. PubMed ID: 31786569
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Turner Syndrome Systematic Review: Spontaneous Thelarche and Menarche Stratified by Karyotype.
    Dabrowski E; Jensen R; Johnson EK; Habiby RL; Brickman WJ; Finlayson C
    Horm Res Paediatr; 2019; 92(3):143-149. PubMed ID: 31918426
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spontaneous pregnancy in a woman with 45,X/47,XXX mosaicism in both serum and germ cell lines. A case report.
    Eblen AC; Nakajima ST
    J Reprod Med; 2003 Feb; 48(2):121-3. PubMed ID: 12621797
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mosaic Turner syndrome shows reduced penetrance in an adult population study.
    Tuke MA; Ruth KS; Wood AR; Beaumont RN; Tyrrell J; Jones SE; Yaghootkar H; Turner CLS; Donohoe ME; Brooke AM; Collinson MN; Freathy RM; Weedon MN; Frayling TM; Murray A
    Genet Med; 2019 Apr; 21(4):877-886. PubMed ID: 30181606
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fertility preservation in Turner syndrome: Karyotype does not predict ovarian response to stimulation.
    Vergier J; Bottin P; Saias J; Reynaud R; Guillemain C; Courbiere B
    Clin Endocrinol (Oxf); 2019 Nov; 91(5):646-651. PubMed ID: 31420888
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Down-Turner syndrome (45,X/47,XY,+21): case report and review].
    Ryu SW; Lee G; Baik CS; Shim SH; Kim JT; Lee JS; Lee KA
    Korean J Lab Med; 2010 Apr; 30(2):195-200. PubMed ID: 20445340
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.