BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

254 related articles for article (PubMed ID: 32506765)

  • 1. The epidemiology of sex chromosome abnormalities.
    Berglund A; Stochholm K; Gravholt CH
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):202-215. PubMed ID: 32506765
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood.
    Zhang B; Lu BY; Yu B; Zheng FX; Zhou Q; Chen YP; Zhang XQ
    J Int Med Res; 2017 Apr; 45(2):621-630. PubMed ID: 28357876
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sex differences in psychiatric disorders: what we can learn from sex chromosome aneuploidies.
    Green T; Flash S; Reiss AL
    Neuropsychopharmacology; 2019 Jan; 44(1):9-21. PubMed ID: 30127341
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Survival in double aneuploidy involving trisomy 18 and sex chromosome trisomy: A case report of a 27-month-old child and a review of the literature.
    Watabe T; Koga H
    Congenit Anom (Kyoto); 2019 Mar; 59(2):43-46. PubMed ID: 29732662
    [No Abstract]   [Full Text] [Related]  

  • 7. Clinical experience regarding the accuracy of NIPT in the detection of sex chromosome abnormality.
    Zheng Y; Wan S; Dang Y; Song T; Chen B; Zhang J
    J Gene Med; 2020 Aug; 22(8):e3199. PubMed ID: 32267591
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sex chromosomes and the brain: a study of neuroanatomy in XYY syndrome.
    Bryant DM; Hoeft F; Lai S; Lackey J; Roeltgen D; Ross J; Reiss AL
    Dev Med Child Neurol; 2012 Dec; 54(12):1149-56. PubMed ID: 23057627
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Gonosomal trisomy syndrome. Five case reports and review of literature].
    Schwemmle C; Jungheim M; Ptok M
    Laryngorhinootologie; 2013 Nov; 92(11):725-31. PubMed ID: 23929211
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Meiotic Behavior of Extra Sex Chromosomes in Patients with the 47,XXY and 47,XYY Karyotype and Its Ultimate Consequences for Spermatogenesis.
    Iqbal F
    Crit Rev Eukaryot Gene Expr; 2020; 30(1):19-37. PubMed ID: 32421982
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dermatoglyphs in sex chromosome anomalies.
    Saldaña-Garcia P
    J Ment Defic Res; 1979 Jun; 23(2):91-104. PubMed ID: 490635
    [No Abstract]   [Full Text] [Related]  

  • 12. [Examination of sex chromosome abnormalities in childhood].
    Pinti É; Lengyel A; Sallai Á; Fekete G; Haltrich I
    Orv Hetil; 2018 Jul; 159(27):1121-1128. PubMed ID: 29961370
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Summary of clinical findings: profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes.
    Robinson A; Lubs HA; Nielsen J; Sørensen K
    Birth Defects Orig Artic Ser; 1979; 15(1):261-6. PubMed ID: 444644
    [No Abstract]   [Full Text] [Related]  

  • 14. Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
    Petersen AK; Cheung SW; Smith JL; Bi W; Ward PA; Peacock S; Braxton A; Van Den Veyver IB; Breman AM
    Am J Obstet Gynecol; 2017 Dec; 217(6):691.e1-691.e6. PubMed ID: 29032050
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey.
    Ataman E; Cogulu O; Durmaz A; Karaca E; Durmaz B; Akin H; Ozkinay F
    Genet Test Mol Biomarkers; 2012 Feb; 16(2):150-3. PubMed ID: 21977968
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gonadal dysfunction and beyond: Clinical challenges in children, adolescents, and adults with 47,XXY Klinefelter syndrome.
    Zitzmann M; Rohayem J
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):302-312. PubMed ID: 32415901
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High false-positive non-invasive prenatal screening results for sex chromosome abnormalities: Are maternal factors the culprit?
    Zhang B; Zhou Q; Chen Y; Shi Y; Zheng F; Liu J; Yu B
    Prenat Diagn; 2020 Mar; 40(4):463-469. PubMed ID: 31318441
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.
    Mountford HS; Bishop DVM; Thompson PA; Simpson NH; Newbury DF
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):256-266. PubMed ID: 32452638
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.
    Tartaglia N; Howell S; Davis S; Kowal K; Tanda T; Brown M; Boada C; Alston A; Crawford L; Thompson T; van Rijn S; Wilson R; Janusz J; Ross J
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):428-443. PubMed ID: 32506668
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21-year single-center experience.
    Elkarhat Z; Belkady B; Charoute H; Zarouf L; Razoki L; Aboulfaraj J; Nassereddine S; Elbakay C; Nasser B; Barakat A; Rouba H
    Am J Med Genet A; 2019 Aug; 179(8):1516-1524. PubMed ID: 31207162
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.