Connection

SAU WAI CHEUNG to Genetic Markers

This is a "connection" page, showing publications SAU WAI CHEUNG has written about Genetic Markers.
Connection Strength

0.148
  1. Correlation between phenotypic expression of de novo marker chromosomes and genomic organization using replicational banding. Prenat Diagn. 1990 Nov; 10(11):717-24.
    View in: PubMed
    Score: 0.075
  2. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center. Ultrasound Obstet Gynecol. 2014 Mar; 43(3):254-64.
    View in: PubMed
    Score: 0.023
  3. Sex chromosome marker: clinical significance and DNA characterization. Am J Med Genet. 1991 Apr 01; 39(1):97-101.
    View in: PubMed
    Score: 0.019
  4. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenet Genome Res. 2009; 124(1):102-5.
    View in: PubMed
    Score: 0.017
  5. Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients. J Appl Genet. 2007; 48(2):167-75.
    View in: PubMed
    Score: 0.014
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.