BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

481 related articles for article (PubMed ID: 12493042)

  • 1. Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects.
    Chaoui R; Kalache KD; Heling KS; Tennstedt C; Bommer C; Körner H
    Ultrasound Obstet Gynecol; 2002 Dec; 20(6):546-52. PubMed ID: 12493042
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The thymic-thoracic ratio in fetal heart defects: a simple way to identify fetuses at high risk for microdeletion 22q11.
    Chaoui R; Heling KS; Lopez AS; Thiel G; Karl K
    Ultrasound Obstet Gynecol; 2011 Apr; 37(4):397-403. PubMed ID: 21308838
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.
    Boudjemline Y; Fermont L; Le Bidois J; Lyonnet S; Sidi D; Bonnet D
    J Pediatr; 2001 Apr; 138(4):520-4. PubMed ID: 11295715
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assessment of the thymus at echocardiography in fetuses at risk for 22q11.2 deletion.
    Barrea C; Yoo SJ; Chitayat D; Valsangiacomo E; Winsor E; Smallhorn JF; Hornberger LK
    Prenat Diagn; 2003 Jan; 23(1):9-15. PubMed ID: 12533805
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signs.
    Volpe P; Marasini M; Caruso G; Marzullo A; Buonadonna AL; Arciprete P; Di Paolo S; Volpe G; Gentile M
    Prenat Diagn; 2003 Sep; 23(9):752-7. PubMed ID: 12975788
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Frequency of 22q11 deletions in patients with conotruncal defects.
    Goldmuntz E; Clark BJ; Mitchell LE; Jawad AF; Cuneo BF; Reed L; McDonald-McGinn D; Chien P; Feuer J; Zackai EH; Emanuel BS; Driscoll DA
    J Am Coll Cardiol; 1998 Aug; 32(2):492-8. PubMed ID: 9708481
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome.
    Gaiser KB; Schindewolf EM; Conway LJ; Coleman BG; Oliver ER; Rychik JR; Debari SE; Mcdonald-Mcginn DM; Zackai EH; Moldenhauer JS; Gebb JS
    Prenat Diagn; 2024 Jun; 44(6-7):796-803. PubMed ID: 38497811
    [TBL] [Abstract][Full Text] [Related]  

  • 8. First-trimester fetal cardiac examination using spatiotemporal image correlation, tomographic ultrasound and color Doppler imaging for the diagnosis of complex congenital heart disease in high-risk patients.
    Turan S; Turan OM; Desai A; Harman CR; Baschat AA
    Ultrasound Obstet Gynecol; 2014 Nov; 44(5):562-7. PubMed ID: 24585667
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
    Ziolkowska L; Kawalec W; Turska-Kmiec A; Krajewska-Walasek M; Brzezinska-Rajszys G; Daszkowska J; Maruszewski B; Burczynski P
    Eur J Pediatr; 2008 Oct; 167(10):1135-40. PubMed ID: 18172682
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
    Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
    Momma K; Kondo C; Matsuoka R
    J Am Coll Cardiol; 1996 Jan; 27(1):198-202. PubMed ID: 8522695
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome.
    Lee MY; Won HS; Baek JW; Cho JH; Shim JY; Lee PR; Kim A
    Obstet Gynecol Sci; 2014 Jan; 57(1):11-6. PubMed ID: 24596813
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reliability of fetal thymus measurement in prediction of 22q11.2 deletion: a retrospective study using four-dimensional spatiotemporal image correlation volumes.
    Bataeva R; Bellsham-Revell H; Zidere V; Allan LD
    Ultrasound Obstet Gynecol; 2013 Feb; 41(2):172-6. PubMed ID: 22605637
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Prenatally detected aortic arch anomalies and their consequences after birth].
    Tidrenczel Z; P Tardy E; Ladányi A; Hajdú J; Böjtös I; Sarkadi E; Simon J; Demeter J
    Orv Hetil; 2023 Jul; 164(28):1111-1120. PubMed ID: 37454329
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Conotruncal anomalies in fetal life: accuracy of diagnosis, associated defects and outcome.
    Galindo A; Mendoza A; Arbues J; Grañeras A; Escribano D; Nieto O
    Eur J Obstet Gynecol Reprod Biol; 2009 Sep; 146(1):55-60. PubMed ID: 19481856
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
    Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Prenatal diagnosis of conotruncal heart diseases. Results in 337 cases].
    Boudjemline Y; Fermont L; Le Bidois J; Fraisse A; Kachaner J; Villain E; Sidi D; Bonnet D
    Arch Mal Coeur Vaiss; 2000 May; 93(5):583-6. PubMed ID: 10858856
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography.
    Bellucco FT; Belangero SI; Farah LM; Machado MV; Cruz AP; Lopes LM; Lopes MA; Zugaib M; Cernach MC; Melaragno MI
    Pediatr Cardiol; 2010 Nov; 31(8):1146-50. PubMed ID: 20848279
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.
    Momma K; Kondo C; Matsuoka R; Takao A
    Am J Cardiol; 1996 Sep; 78(5):591-4. PubMed ID: 8806353
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of a 22q11 deletion in a second-trimester fetus with conotruncal anomaly, absent thymus and meningomyelocele: Kousseff syndrome.
    Canda MT; Demir N; Bal FU; Doganay L; Sezer O
    J Obstet Gynaecol Res; 2012 Apr; 38(4):737-40. PubMed ID: 22380655
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.