The Fetal Medicine Foundation 14th World Congress in Fetal Medicine
Abstracts
 
  • Aneuploidy
  • cf DNA in maternal blood
  • Defects
    • CNS
    • Face
    • Heart
    • Lungs
    • Abdominal wall
    • GIT
    • Renal
    • Genitalia
    • Skeleton
    • High NT
    • Tumor
    • Syndromes
    • All
  • Fetal anemia
  • Impaired placentation
  • Diabetes / macrosomia
  • Preterm birth
  • Growth scan
  • Placental problems
  • Amniotic fluid abnormalities
  • Labor / delivery
  • Infections
  • Maternal
    • Maternal age
    • Obstetric cholestasis
    • Maternal death
    • Other conditions
  • Twins
  • Other

Aneuploidy

  1. Fetal loss following second trimester amniocentesis. Who is at greater risk? View pdf
  2. Decision for amniocenetsis: The impact of screening tests after the age of 35 View pdf
  3. Determination of the median levels of maternal serum free bhCG, PAPP-A and fetal NT at 11-13+6 weeks View pdf
  4. Prenatal diagnosis of trisomy 9 View pdf
  5. The risk of 22q11. 2 deletion in fetuses with a right aortic arch and a normal heart View pdf
  6. The association between fetal atrioventricular septal defect and chromosomal abnormalities in the current era View pdf
  7. Normative value of fetal nasal bone length in chromosomally normal fetuses at 11–16 weeks of gestation View pdf
  8. Prenasal thickness at 16–23 weeks of gestation in a Turkish population View pdf
  9. A case of Turner syndrome diagnosed through puncture of the cystic hygroma View pdf
  10. First trimester combined test improved the performance of screening for trisomy 21; population data View pdf
  11. Echogenic intracardial focus- soft marker for aneuploidy. But if EIF isn´t EIF? View pdf
  12. First trimester diagnosis of cystic hygromata by transvaginal ultrasound and cytogenetic evaluation View pdf
  13. Prevalence of CNVs for isolated and multiple structural abnormalities using chromosomal microarray analysis View pdf
  14. A case of derivative chromosome 22 due to paternal t(Y;22) translocation in a female fetus View pdf
  15. Chromosome aberration detected by amniocentesis View pdf
  16. Prenatal diagnosis of rare familial unbalanced translocation of chromosomes 7 and 12 View pdf
  17. First trimester combined screening of trisomy 21: two years practice of the first hospital experience in Tunisia View pdf
  18. Perinatal diagnosis of chromosomal aneuploidies View pdf
  19. Combined first trimester trisomy 21 screening: comparison study between Siemens and Roche solutions View pdf
  20. Target training based on audit and feendback improves nuchal translucency ultrasound image quality View pdf
  21. Characteristics of first trimester screening non-responders in a high up-take population View pdf
  22. First case of prenatal diagnosis of trisomy 9 in Tunisia View pdf
  23. Prenatal diagnosis of familial pericentric inv(16) in a ultrasonographically normal fetus View pdf
  24. Prenatal diagnosis of partial trisomy 3q with multiple anomalies due to maternal balanced translocation View pdf
  25. Performance of universal first trimester combined screening at public hospitals in Hong Kong View pdf
  26. Does the size of the spine needle have any influence on pain experience during mid-trimester amniocentesis View pdf
  27. Defining fetal nasal bone in the First Trimester View pdf
  28. A case of trisomy 13 View pdf
  29. On the Origin of the Origin of Down Syndrome (DS) View pdf
  30. Women's and healthcare professionals' preferences for prenatal testing: a discrete choice experiment View pdf
114211411137113411141031983978958907892879873846821807804803800753746745733732680670660645642622
© 2015 The Fetal Medicine Foundation