Connection

SAU WAI CHEUNG to Middle Aged

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

0.121
  1. Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review. BMC Med Genet. 2015 Mar 14; 16:12.
    View in: PubMed
    Score: 0.028
  2. Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases. Am J Med Genet A. 2008 Sep 01; 146A(17):2242-51.
    View in: PubMed
    Score: 0.018
  3. A retrospective study of preimplantation embryos diagnosed with monosomy by fluorescence in situ hybridization (FISH). Cytogenet Genome Res. 2006; 114(3-4):359-66.
    View in: PubMed
    Score: 0.015
  4. Residual lymph node tumour burden following removal of a single axillary sentinel lymph with macrometastatic disease in women with screen-detected invasive breast cancer. BJS Open. 2021 03 05; 5(2).
    View in: PubMed
    Score: 0.011
  5. Contralateral breast cancer: incidence according to ductal or lobular phenotype of the primary. Clin Radiol. 2016 Feb; 71(2):159-63.
    View in: PubMed
    Score: 0.007
  6. Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite. BMC Med Genet. 2014 Dec 04; 15:128.
    View in: PubMed
    Score: 0.007
  7. CYP2B6-G516T genotype influences plasma efavirenz concentration in a Hong Kong population, allowing potential individualization of therapy. HIV Med. 2014 Jan; 15(1):63-4.
    View in: PubMed
    Score: 0.006
  8. Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. Nat Genet. 2012 Apr 29; 44(6):639-41.
    View in: PubMed
    Score: 0.006
  9. Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions. J Clin Endocrinol Metab. 2011 Apr; 96(4):E674-9.
    View in: PubMed
    Score: 0.005
  10. Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems. Am J Hum Genet. 2010 Dec 10; 87(6):857-65.
    View in: PubMed
    Score: 0.005
  11. Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men. J Urol. 2010 Apr; 183(4):1636-42.
    View in: PubMed
    Score: 0.005
  12. A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nat Genet. 2009 Dec; 41(12):1269-71.
    View in: PubMed
    Score: 0.005
  13. Ciprofloxacin in the management of pulmonary tuberculosis in the face of hepatic dysfunction. Drugs Exp Clin Res. 1995; 21(2):79-83.
    View in: PubMed
    Score: 0.002
  14. Ofloxacin penetration into tuberculous pleural effusion. Antimicrob Agents Chemother. 1991 Oct; 35(10):2159-60.
    View in: PubMed
    Score: 0.001
  15. Variance of plasma free and esterified cholesterol in adult twins. Am J Hum Genet. 1976 Mar; 28(2):174-8.
    View in: PubMed
    Score: 0.000
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.