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 *

317 related articles for article (PubMed ID: 16131369)

  • 1. Iniencephaly and chromosome mosaicism: a report of two cases.
    Halder A; Agarwal S; Pandey A
    Congenit Anom (Kyoto); 2005 Sep; 45(3):102-5. PubMed ID: 16131369
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cryptic mosaicism for monosomy 20 identified in renal tract cells.
    Stefanou EG; Crocker M; Boon A; Stewart H
    Clin Genet; 2006 Sep; 70(3):228-32. PubMed ID: 16922725
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism.
    Nowaczyk MJ; Ramsay JA; Mohide P; Tomkins DJ
    Am J Med Genet; 1998 May; 77(4):306-9. PubMed ID: 9600741
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Chromosomal mosaicism in spontaneous abortions: analysis of 650 cases].
    Vorsanova SG; Iurov IIu; Kolotiĭ AD; Beresheva AK; Demidova IA; Kurinnaia OS; Kravets VS; Monakhov VV; Solov'ev IV; Iurov IuB
    Genetika; 2010 Oct; 46(10):1356-9. PubMed ID: 21254555
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neural tube defects in chromosomally normal and abnormal human embryos.
    Coerdt W; Miller K; Holzgreve W; Rauskolb R; Schwinger E; Rehder H
    Ultrasound Obstet Gynecol; 1997 Dec; 10(6):410-5. PubMed ID: 9476327
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus.
    Schlegel M; Baumer A; Riegel M; Wiedemann U; Schinzel A
    Prenat Diagn; 2002 May; 22(5):418-21. PubMed ID: 12001199
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal abnormalities in fetuses with open neural tube defects: prenatal identification with ultrasound.
    Sepulveda W; Corral E; Ayala C; Be C; Gutierrez J; Vasquez P
    Ultrasound Obstet Gynecol; 2004 Apr; 23(4):352-6. PubMed ID: 15065184
    [TBL] [Abstract][Full Text] [Related]  

  • 10. First trimester diagnosis of iniencephaly associated with fetal malformations and trisomy 18: report of a new case and gene analysis on folate metabolism in parents.
    Tonni G; Azzoni D; Panteghini M; Ventura A; Cavalli P
    Congenit Anom (Kyoto); 2007 Sep; 47(3):101-4. PubMed ID: 17688469
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
    Iourov IY; Soloviev IV; Vorsanova SG; Monakhov VV; Yurov YB
    J Histochem Cytochem; 2005 Mar; 53(3):401-8. PubMed ID: 15750029
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
    Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis.
    Vorsanova SG; Kolotii AD; Iourov IY; Monakhov VV; Kirillova EA; Soloviev IV; Yurov YB
    J Histochem Cytochem; 2005 Mar; 53(3):375-80. PubMed ID: 15750024
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome.
    Gersak K; Writzl K; Veble A; Liehr T
    Genet Couns; 2010; 21(3):335-42. PubMed ID: 20964126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report.
    Phadke SR; Thakur S
    Prenat Diagn; 2002 Dec; 22(13):1240-1. PubMed ID: 12478643
    [No Abstract]   [Full Text] [Related]  

  • 16. Chromosomal abnormalities associated with neural tube defects (I): full aneuploidy.
    Chen CP
    Taiwan J Obstet Gynecol; 2007 Dec; 46(4):325-35. PubMed ID: 18182338
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Trisomy/partial monosomy 13 mosaicism associated with relatively mild clinical malformation.
    Duckett DP; Porter HJ; Young ID
    Ann Genet; 1992; 35(2):113-6. PubMed ID: 1524408
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Examination of trisomy 13, 18 and 21 foetal tissues at different gestational ages using FISH.
    Moore GE; Ruangvutilert P; Chatzimeletiou K; Bell G; Chen CK; Johnson P; Harper JC
    Eur J Hum Genet; 2000 Mar; 8(3):223-8. PubMed ID: 10780789
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.