Connection

IGNATIA VAN DEN VEYVER to In Situ Hybridization, Fluorescence

This is a "connection" page, showing publications IGNATIA VAN DEN VEYVER has written about In Situ Hybridization, Fluorescence.
  1. Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature. Prenat Diagn. 2012 Apr; 32(4):351-61.
    View in: PubMed
    Score: 0.068
  2. Copy-number changes in prenatal diagnosis. Expert Rev Mol Diagn. 2011 Jul; 11(6):579-92.
    View in: PubMed
    Score: 0.064
  3. Applications of array comparative genomic hybridization in obstetrics. Obstet Gynecol Clin North Am. 2010 Mar; 37(1):71-85, Table of Contents.
    View in: PubMed
    Score: 0.059
  4. Recurrent biparental hydatidiform mole: additional evidence for a 1.1-Mb locus in 19q13.4 and candidate gene analysis. J Soc Gynecol Investig. 2005 Jul; 12(5):376-83.
    View in: PubMed
    Score: 0.043
  5. Applied molecular genetic techniques for prenatal diagnosis. Curr Opin Obstet Gynecol. 1998 Apr; 10(2):97-103.
    View in: PubMed
    Score: 0.026
  6. Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory. Am J Obstet Gynecol. 2017 12; 217(6):691.e1-691.e6.
    View in: PubMed
    Score: 0.025
  7. Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women. Prenat Diagn. 2016 Dec; 36(12):1127-1134.
    View in: PubMed
    Score: 0.023
  8. Prenatal diagnosis and clinical findings in a case of hexasomy 12p. Am J Med Genet. 1993 Dec 01; 47(8):1171-4.
    View in: PubMed
    Score: 0.019
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.