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 *

199 related articles for article (PubMed ID: 21213493)

  • 21. [Fetal diagnosis of Edwards syndrome].
    Tóth A; Hajdu K; Intödy Z; Rajczy K; László J
    Orv Hetil; 1990 Oct; 131(43):2355-6, 2359-60. PubMed ID: 2234934
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of de novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born.
    Fernández-Novoa MC; Vargas MT; Granell MR; Carreto P
    Prenat Diagn; 2004 Jun; 24(6):414-7. PubMed ID: 15229838
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Second trimester ultrasound screening for chromosomal abnormalities.
    Shipp TD; Benacerraf BR
    Prenat Diagn; 2002 Apr; 22(4):296-307. PubMed ID: 11981910
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Ultrasonographically detectable markers of fetal chromosomal abnormalities.
    Nicolaides KH; Snijders RJ; Gosden CM; Berry C; Campbell S
    Lancet; 1992 Sep; 340(8821):704-7. PubMed ID: 1355807
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Placental volume measured by three-dimensional ultrasound at 11 to 13 + 6 weeks of gestation: relation to chromosomal defects.
    Wegrzyn P; Faro C; Falcon O; Peralta CF; Nicolaides KH
    Ultrasound Obstet Gynecol; 2005 Jul; 26(1):28-32. PubMed ID: 15937964
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Contribution of 3D ultrasound and fetal face studies to the prenatal diagnosis of Pallister-Killian syndrome.
    Sananes N; Guigue V; Vayssiere C; Kohler M; Girard-Lemaire F; Flori E; Carelle-Calmels N; Boehm N; Samama B; Doray B; Favre R
    J Matern Fetal Neonatal Med; 2010 Jun; 23(6):558-62. PubMed ID: 19718583
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Usefulness of ultrasonographic markers in chromosomal abnormalities].
    Rivera Muñoz JE; Leis Márquez MT; García-Cavazos RJ; Hernández Andrade EA; Guzmán Huerta ME; Rodríguez-Bosch MR
    Ginecol Obstet Mex; 1997 Sep; 65():394-9. PubMed ID: 9410812
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Prenatal diagnosis. Review, personal and prospective studies].
    Engel E; Empson J; DeLozier D; McGee B; da Costa Woodson E; Engel-de Montmollin M; Carter T; Lorber C; Cassidy SB; Millis J; Heller RM; Boehm F; Vanhooydonk J
    Schweiz Med Wochenschr; 1979 Jul; 109(27):998-1010. PubMed ID: 88763
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Karyotyping of fetuses with developmental disorders. A 5-year material 1985-89].
    Tuveng JM; Eik-Nes SH; Sviggum O; Isaksen C; Berg K; Leren TP; van der Hagen CB
    Tidsskr Nor Laegeforen; 1993 Jan; 113(3):339-42. PubMed ID: 8441983
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Prevalence of congenital abnormalities identified in fetuses with 13, 18 and 21 chromosomal trisomy].
    Emer CS; Duque JA; Müller AL; Gus R; Sanseverino MT; da Silva AA; Magalhães JA
    Rev Bras Ginecol Obstet; 2015 Jul; 37(7):333-8. PubMed ID: 26247254
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detection of chromosome aberrations in the second trimester using genetic amniocentesis: experience during 1995-2004.
    Tseng JJ; Chou MM; Lo FC; Lai HY; Chen MH; Ho ES
    Taiwan J Obstet Gynecol; 2006 Mar; 45(1):39-41. PubMed ID: 17272206
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 3-D ultrasound of the fetal ear and fetal autosomal trisomies: a pilot study of a new screening protocol.
    Ginsberg NA; Cohen L; Dungan JS; Concialdi S; Mangers K; Shulman LP
    Prenat Diagn; 2011 Mar; 31(3):311-4. PubMed ID: 21294134
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. Fetal facial defects: associated malformations and chromosomal abnormalities.
    Nicolaides KH; Salvesen DR; Snijders RJ; Gosden CM
    Fetal Diagn Ther; 1993; 8(1):1-9. PubMed ID: 8452644
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fetal lateral ventricle choroid plexus cysts: the dilemma of amniocentesis.
    Achiron R; Barkai G; Katznelson MB; Mashiach S
    Obstet Gynecol; 1991 Nov; 78(5 Pt 1):815-8. PubMed ID: 1923204
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Transvaginal sonographic measurement of fetal lingual width in early pregnancy.
    Bronshtein M; Zimmer EZ; Tzidony D; Hajos J; Jaeger M; Blazer S
    Prenat Diagn; 1998 Jun; 18(6):577-80. PubMed ID: 9664602
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Antenatal diagnosis of fetal abnormality with special reference to amniocentesis.
    Turnbull AC; Gregory PJ; Laurence KM
    Proc R Soc Med; 1973 Nov; 66(11):1115-8. PubMed ID: 4273030
    [No Abstract]   [Full Text] [Related]  

  • 38. The ultrasound triad of fetal hydramnios, abnormal hand posturing, and any other anomaly predicts autosomal trisomy.
    Carlson DE; Platt LD; Medearis AL
    Obstet Gynecol; 1992 May; 79(5 ( Pt 1)):731-4. PubMed ID: 1533021
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe.
    De Vigan C; Baena N; Cariati E; Clementi M; Stoll C;
    Ann Genet; 2001; 44(4):209-17. PubMed ID: 11755107
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis of trisomy 18 as true mosaicism by three-dimensional ultrasonography: a case report.
    Guimarães Filho HA; Araujo Júnior E; Mattar R; Pires CR; Zanforlin Filho SM; Moron AF; Nardozza LM
    Arch Gynecol Obstet; 2007 Feb; 275(2):133-5. PubMed ID: 16721579
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.