Connection

SANDRA DARILEK to Female

This is a "connection" page, showing publications SANDRA DARILEK has written about Female.
Connection Strength

0.105
  1. Telegenetics to provide comprehensive prenatal diagnosis. Prenat Diagn. 2024 04; 44(4):492-498.
    View in: PubMed
    Score: 0.036
  2. Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives. Genet Med. 2008 Jan; 10(1):13-8.
    View in: PubMed
    Score: 0.012
  3. Hereditary multiple exostosis and pain. J Pediatr Orthop. 2005 May-Jun; 25(3):369-76.
    View in: PubMed
    Score: 0.010
  4. Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2023 02; 25(2):100336.
    View in: PubMed
    Score: 0.008
  5. Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum. Am J Med Genet A. 2019 03; 179(3):386-396.
    View in: PubMed
    Score: 0.006
  6. Attitudes Toward and Uptake of Prenatal Genetic Screening and Testing in Twin Pregnancies. J Genet Couns. 2018 09; 27(5):1238-1247.
    View in: PubMed
    Score: 0.006
  7. Genesurance Counseling: Patient Perspectives. J Genet Couns. 2018 08; 27(4):814-822.
    View in: PubMed
    Score: 0.006
  8. Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. J Womens Health (Larchmt). 2017 07; 26(7):755-761.
    View in: PubMed
    Score: 0.006
  9. Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes. Fam Cancer. 2010 Sep; 9(3):479-87.
    View in: PubMed
    Score: 0.004
  10. Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenat Diagn. 2009 Jan; 29(1):29-39.
    View in: PubMed
    Score: 0.003
  11. DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls. Am J Med Genet A. 2006 Nov 15; 140(22):2401-15.
    View in: PubMed
    Score: 0.003
  12. Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med. 2006 Nov; 8(11):719-27.
    View in: PubMed
    Score: 0.003
  13. 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: 0.003
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.