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 *

90 related articles for article (PubMed ID: 3057974)

  • 21. A fetus with partial trisomy 3 (p21-pter) detected by prenatal diagnosis.
    Suzumori K; Koishi T; Manzai M; Yagami Y
    Jinrui Idengaku Zasshi; 1983 Mar; 28(1):45-53. PubMed ID: 6876482
    [No Abstract]   [Full Text] [Related]  

  • 22. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Echographic detection of chromosomal anomalies apropos of trisomy 13 and 18].
    Aubry JP; Aubry MC; Henrion R; Boué J; Labbe F
    J Genet Hum; 1982 Oct; 30(3):233-53. PubMed ID: 7153769
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A rare case of de novo distal 19q trisomy prenatally diagnosed.
    Rombout S; Sartenaer D; Parmentier B; Dugauquier C; Gillerot Y
    Prenat Diagn; 2004 Oct; 24(10):822-7. PubMed ID: 15503276
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Fetal heart rate monitoring casebook. Fetal heart rate monitoring in fetuses with congenital anomalies.
    Gimovsky ML; Dalpe J
    J Perinatol; 1998; 18(1):81-4. PubMed ID: 9527952
    [No Abstract]   [Full Text] [Related]  

  • 26. Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome.
    Peng HH; Wang TH; Hsueh DW; Chang SD; Soong YK
    Prenat Diagn; 2005 Jun; 25(6):470-4. PubMed ID: 15966037
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Familial 4;18 chromosome translocation resulting in trisomy 4p and monosomy 18p: affected individuals with discordant phenotype.
    Berman DR; Couyoumjian CA; Treadwell MC; Barr M
    Prenat Diagn; 2009 May; 29(5):538-40. PubMed ID: 19226522
    [No Abstract]   [Full Text] [Related]  

  • 28. Positive biochemical screening for trisomy 18: on the path of trisomy 9.
    Póvoa A; Ramalho C; Torgal A; Brandão O; Matias A; Oliveira MJ; Montenegro N; Castedo S
    Prenat Diagn; 2008 Feb; 28(2):162-4. PubMed ID: 18236431
    [No Abstract]   [Full Text] [Related]  

  • 29. Trisomy 13 and trisomy 18 in a defined population: epidemiological, genetic and prenatal observations.
    Parker MJ; Budd JL; Draper ES; Young ID
    Prenat Diagn; 2003 Oct; 23(10):856-60. PubMed ID: 14558033
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A; Röddiger S; Born HJ; Baier P; Halberstadt E
    Z Geburtshilfe Neonatol; 1996; 200(5):186-90. PubMed ID: 9035828
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spontaneous loss of fetuses with chromosomally unbalanced D/21--or reciprocal translocations in late pregnancy.
    Daniel A
    Am J Med Genet; 1989 Jun; 33(2):285. PubMed ID: 2764041
    [No Abstract]   [Full Text] [Related]  

  • 32. The fetal phenotype in 15q2 duplication.
    Fryns JP; Kleczkowska A; Moerman P; Vandenberghe K; Van den Berghe H
    Ann Genet; 1988; 31(2):123-5. PubMed ID: 3261148
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Ultrasonic findings with holoprosencephaly.
    Hill LM; Breckle R; Bonebrake CR
    J Reprod Med; 1982 Mar; 27(3):172-5. PubMed ID: 7086766
    [No Abstract]   [Full Text] [Related]  

  • 34. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
    Ogilvie CM; Donaghue C; Fox SP; Docherty Z; Mann K
    J Histochem Cytochem; 2005 Mar; 53(3):285-8. PubMed ID: 15750003
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Application of inter-fluorescence in situ hybridization of chromosome 13/21 alpha satellite probe in amniotic cells for prenatal diagnosis trisomy 21 syndrome].
    Li W; Wu Y; Ye Z
    Zhonghua Fu Chan Ke Za Zhi; 2001 Feb; 36(2):76-8. PubMed ID: 11783350
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis of complete trisomy 9: a case report and review of the literature.
    Kor-Anantakul O; Suwanrath C; Kanngurn S; Rujirabanjerd S; Suntharasaj T; Pinjaroen S
    Am J Perinatol; 2006 Feb; 23(2):131-5. PubMed ID: 16506121
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of partial trisomy 21 associated with maternal balanced translocation 46xx der 21 t(21q;22q) with pericentric inversion of chromosome 9.
    Parmar RC; Sira P
    J Postgrad Med; 2003; 49(2):154-6. PubMed ID: 12867693
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis of a fetus with partial trisomy 7p.
    Ozgun MT; Batukan C; Basbug M; Akgun H; Caglayan O; Dundar M
    Fetal Diagn Ther; 2007; 22(3):229-32. PubMed ID: 17228165
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [The prenatal detection of trisomy 13, 18, and 21: comparison of the advanced first trimester screening (AFS) with the first trimester screening according to Nicolaides].
    Hörmansdörfer C; Schmidt P; Hillemanns P; Scharf A
    Z Geburtshilfe Neonatol; 2007 Dec; 211(6):243-9. PubMed ID: 18176905
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
    Santolaya-Forgas J; De Leon J; Powell WC; Tonk V
    Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.