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 *

130 related articles for article (PubMed ID: 25696020)

  • 1. A case report of a fetus with mosaic autosomal variegated aneuploidies and literature review.
    Cho CH; Oh MJ; Lim CS; Lee CK; Cho Y; Yoon SY
    Ann Clin Lab Sci; 2015; 45(1):106-9. PubMed ID: 25696020
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Syndrome of microcephaly, Dandy-Walker malformation, and Wilms tumor caused by mosaic variegated aneuploidy with premature centromere division (PCD): report of a new case and review of the literature.
    Kawame H; Sugio Y; Fuyama Y; Hayashi Y; Suzuki H; Kurosawa K; Maekawa K
    J Hum Genet; 1999; 44(4):219-24. PubMed ID: 10429359
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
    Chen CP; Lee CC; Chen WL; Wang W; Tzen CY
    Prenat Diagn; 2004 Jan; 24(1):19-25. PubMed ID: 14755404
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mosaic variegated aneuploidy without microcephaly: implications for cytogenetic diagnosis.
    Micale MA; Schran D; Emch S; Kurczynski TW; Rahman N; Van Dyke DL
    Am J Med Genet A; 2007 Aug; 143A(16):1890-3. PubMed ID: 17632782
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and genetic heterogeneity in patients with mosaic variegated aneuploidy: delineation of clinical subtypes.
    García-Castillo H; Vásquez-Velásquez AI; Rivera H; Barros-Núñez P
    Am J Med Genet A; 2008 Jul; 146A(13):1687-95. PubMed ID: 18548531
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Refractory infantile spasms associated with mosaic variegated aneuploidy syndrome.
    Akasaka N; Tohyama J; Ogawa A; Takachi T; Watanabe A; Asami K
    Pediatr Neurol; 2013 Nov; 49(5):364-7. PubMed ID: 23916859
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization, and literature review.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen YT; Kuo YL; Chen WL; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):79-85. PubMed ID: 24767652
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of premature chromatid separation/mosaic variegated aneuploidy (PCS/MVA) syndrome.
    Yamaguchi T; Yamaguchi M; Akeno K; Fujisaki M; Sumiyoshi K; Ohashi M; Sameshima H; Ozaki M; Kato M; Kato T; Hosoba E; Kurahashi H
    J Obstet Gynaecol Res; 2018 Jul; 44(7):1313-1317. PubMed ID: 29673003
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Follow-up of two adult brothers with homozygous CEP57 pathogenic variants expands the phenotype of Mosaic Variegated Aneuploidy Syndrome.
    Dery T; Chatron N; Alqahtani A; Pugeat M; Till M; Edery P; Sanlaville D; Schluth-Bolard C; Nicolino M; Lesca G; Putoux A
    Eur J Med Genet; 2020 Nov; 63(11):104044. PubMed ID: 32861809
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome.
    Callier P; Faivre L; Cusin V; Marle N; Thauvin-Robinet C; Sandre D; Rousseau T; Sagot P; Lacombe E; Faber V; Mugneret F
    Am J Med Genet A; 2005 Aug; 137(2):204-7. PubMed ID: 16059936
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of tetrasomy 9p in a 19-week-old fetus with Dandy-Walker malformation: a case report.
    Deurloo KL; Cobben JM; Heins YM; de Ru M; Wijnaendts LC; van Vugt JM
    Prenat Diagn; 2004 Oct; 24(10):796-8. PubMed ID: 15503289
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R; Pfeiffer RA; Kollert A; Beinder E
    Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
    Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literature.
    Schubert R; Eggermann T; Hofstaetter C; von Netzer B; Knöpfle G; Schwanitz G
    Am J Med Genet; 2002 Jul; 110(3):278-82. PubMed ID: 12116238
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
    Christian SL; Smith AC; Macha M; Black SH; Elder FF; Johnson JM; Resta RG; Surti U; Suslak L; Verp MS; Ledbetter DH
    Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly.
    Chen CP; Chern SR; Lee CC; Chen WL; Wang W
    Prenat Diagn; 2001 Feb; 21(2):102-5. PubMed ID: 11241535
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA; Wolff DJ; Dickerman LH; Redline R; Conroy JM; Schwartz S
    Prenat Diagn; 1996 Oct; 16(10):893-7. PubMed ID: 8938057
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Role of FISH on uncultured amniocytes for the diagnosis of aneuploidies in the presence of fetal anomalies.
    Locatelli A; Mariani S; Ciriello E; Dalprà L; Villa N; Sala E; Vergani P
    Fetal Diagn Ther; 2005; 20(1):1-4. PubMed ID: 15608449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
    Chen CP; Peng CR; Chern SR; Kuo YL; Wu PS; Town DD; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel CEP57 variant associated with mosaic variegated aneuploidy syndrome in a Chinese female presenting with short stature, microcephaly, brachydactyly, and small teeth.
    Feng B; Chang G; Zhang Q; Li X; Tang Y; Gu S; Wang Y; Wang J; Wang X
    Mol Genet Genomic Med; 2022 Jun; 10(6):e1951. PubMed ID: 35434947
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.