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Journal Abstract Search

299 related items for PubMed ID: 27644018

  • 21. Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY.
    Tartaglia NR, Ayari N, Hutaff-Lee C, Boada R.
    J Dev Behav Pediatr; 2012 May; 33(4):309-18. PubMed ID: 22333574
    [Abstract] [Full Text] [Related]

  • 22. Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospital.
    Yao H, Jiang F, Hu H, Gao Y, Zhu Z, Zhang H, Wang Y, Guo Y, Liu L, Yuan Y, Zhou L, Wang J, Du B, Qu N, Zhang R, Dong Y, Xu H, Chen F, Jiang H, Liu Y, Zhang L, Tian Z, Liu Q, Zhang C, Pan X, Yang S, Zhao L, Wang W, Liang Z.
    Ultrasound Obstet Gynecol; 2014 Jul; 44(1):17-24. PubMed ID: 24616044
    [Abstract] [Full Text] [Related]

  • 23. Maternal 47,XX,i(X)(q10) as a cause of false positive sex chromosome aneuploidy in noninvasive prenatal screening.
    DeMaio A, Green A, Daly S.
    Prenat Diagn; 2016 Jul; 36(7):693-5. PubMed ID: 27152665
    [No Abstract] [Full Text] [Related]

  • 24. Population-based trends in the prenatal diagnosis of sex chromosome aneuploidy before and after non-invasive prenatal testing.
    Howard-Bath A, Poulton A, Halliday J, Hui L.
    Prenat Diagn; 2018 Dec; 38(13):1062-1068. PubMed ID: 30255507
    [Abstract] [Full Text] [Related]

  • 25. The behavioral profile of children aged 1-5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY).
    Urbanus E, Swaab H, Tartaglia N, Cordeiro L, van Rijn S.
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):444-455. PubMed ID: 32432413
    [Abstract] [Full Text] [Related]

  • 26. The psychiatric phenotype in triple X syndrome: new hypotheses illustrated in two cases.
    Otter M, Schrander-Stumpel CT, Didden R, Curfs LM.
    Dev Neurorehabil; 2012 Jun; 15(3):233-8. PubMed ID: 22582855
    [Abstract] [Full Text] [Related]

  • 27. Screening of fetal chromosomal aneuploidy diseases using noninvasive prenatal testing in twin pregnancies.
    Yu W, Lv Y, Yin S, Liu H, Li X, Liang B, Kong L, Liu C.
    Expert Rev Mol Diagn; 2019 Feb; 19(2):189-196. PubMed ID: 30582381
    [Abstract] [Full Text] [Related]

  • 28. Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis.
    Wigby K, Cordeiro L, Wilson R, Angkustsiri K, Simon TJ, Tartaglia N.
    Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):456-468. PubMed ID: 32548885
    [Abstract] [Full Text] [Related]

  • 29. Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X.
    Yao H, Zhang L, Zhang H, Jiang F, Hu H, Chen F, Jiang H, Mu F, Zhao L, Liang Z, Wang W.
    Prenat Diagn; 2012 Nov; 32(11):1114-6. PubMed ID: 22903289
    [No Abstract] [Full Text] [Related]

  • 30. 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
    [Abstract] [Full Text] [Related]

  • 31. DOUBLE TRISOMY MOSAICISM 48,XXX,+8/46,XX IN A FEMALE: THE FIRST REPORTED CASE.
    Attig A, Ben Jemaa L, Kraoua L, Jilani H, Maazoul F, Mrad R.
    Genet Couns; 2016 Jun; 27(3):441-446. PubMed ID: 30204977
    [No Abstract] [Full Text] [Related]

  • 32. [Phenotypic variability in 47, XXX patients: Clinical report of four new cases].
    Goldschmidt E, Márquez M, Solari A, Ziembar MI, Laudicina A.
    Arch Argent Pediatr; 2010 Aug; 108(4):e88-91. PubMed ID: 20672182
    [Abstract] [Full Text] [Related]

  • 33. Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study.
    Gruchy N, Blondeel E, Le Meur N, Joly-Hélas G, Chambon P, Till M, Herbaux M, Vigouroux-Castera A, Coussement A, Lespinasse J, Amblard F, Jimenez Pocquet M, Lebel-Roy C, Carré-Pigeon F, Flori E, Mugneret F, Jaillard S, Yardin C, Harbuz R, Collonge-Rame MA, Vago P, Valduga M, Leporrier N, Vialard F.
    Prenat Diagn; 2016 Jun; 36(6):523-9. PubMed ID: 27018091
    [Abstract] [Full Text] [Related]

  • 34. Intracortical myelin across laminae in adult individuals with 47,XXX: a 7 Tesla MRI study.
    Serrarens C, Ruiz-Fernandez J, Otter M, Campforts BCM, Stumpel CTRM, Linden DEJ, van Amelsvoort TAMJ, Kashyap S, Vingerhoets C.
    Cereb Cortex; 2024 Aug 01; 34(8):. PubMed ID: 39183364
    [Abstract] [Full Text] [Related]

  • 35. Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX.
    van Rijn S, Swaab H.
    Genes Brain Behav; 2015 Feb 01; 14(2):200-8. PubMed ID: 25684214
    [Abstract] [Full Text] [Related]

  • 36. GnRH-dependent precocious puberty manifested at the age of 14 months in a girl with 47,XXX karyotype.
    Skordis N, Ferrari E, Antoniadou A, Phylactou LA, Fanis P, Neocleous V.
    Hormones (Athens); 2017 Jul 01; 16(3):318-321. PubMed ID: 29278519
    [Abstract] [Full Text] [Related]

  • 37. Noninvasive prenatal screening in southeast China: clinical application and accuracy evaluation.
    Wen L, Gao J, Huang L, Li D, Zhong G.
    Expert Rev Mol Diagn; 2022 Aug 01; 22(8):841-848. PubMed ID: 36107698
    [Abstract] [Full Text] [Related]

  • 38. Behavioral and psychological features in girls and women with triple-X syndrome.
    Freilinger P, Kliegel D, Hänig S, Oehl-Jaschkowitz B, Henn W, Meyer J.
    Am J Med Genet A; 2018 Nov 01; 176(11):2284-2291. PubMed ID: 30070765
    [Abstract] [Full Text] [Related]

  • 39. Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy.
    Boyd PA, Loane M, Garne E, Khoshnood B, Dolk H, EUROCAT working group.
    Eur J Hum Genet; 2011 Feb 01; 19(2):231-4. PubMed ID: 20736977
    [Abstract] [Full Text] [Related]

  • 40. Gene Copy Number Quantification of SHOX, VAMP7, and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates.
    Ibarra-Ramírez M, Lugo-Trampe JJ, Campos-Acevedo LD, Zamudio-Osuna M, Torres-Muñoz I, Gómez-Puente V, García-Castañeda G, Arredondo-Vázquez P, Rodríguez-Sánchez IP, Schaeffer SE, Velasco-Sepúlveda BH, Villarreal-Pérez JZ, Martínez-de-Villarreal LE.
    Genet Test Mol Biomarkers; 2020 Jun 01; 24(6):352-358. PubMed ID: 32423256
    [Abstract] [Full Text] [Related]

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