Connection

RACHEL FRANCISKOVICH to Phenotype

This is a "connection" page, showing publications RACHEL FRANCISKOVICH has written about Phenotype.
Connection Strength

0.161
  1. Short stature and growth hormone deficiency in a subset of patients with Potocki-Lupski syndrome: Expanding the phenotype of PTLS. Am J Med Genet A. 2020 09; 182(9):2077-2084.
    View in: PubMed
    Score: 0.081
  2. Case Series of Nizon-Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid-Triploid Mosaicism. Am J Med Genet A. 2026 01; 200(1):205-214.
    View in: PubMed
    Score: 0.029
  3. Sequence variants in HECTD1 result in a variable neurodevelopmental disorder. Am J Hum Genet. 2025 03 06; 112(3):537-553.
    View in: PubMed
    Score: 0.028
  4. DNA methylation episignature in Gabriele-de Vries?syndrome. Genet Med. 2022 04; 24(4):905-914.
    View in: PubMed
    Score: 0.023
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.