Connection

ALISON BERTUCH to Syndrome

This is a "connection" page, showing publications ALISON BERTUCH has written about Syndrome.
Connection Strength

0.364
  1. The germline p53 activation syndrome: A new patient further refines the clinical phenotype. Am J Med Genet A. 2022 07; 188(7):2204-2208.
    View in: PubMed
    Score: 0.159
  2. The molecular genetics of the telomere biology disorders. RNA Biol. 2016 08 02; 13(8):696-706.
    View in: PubMed
    Score: 0.101
  3. Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM-associated syndromes. Am J Med Genet A. 2023 07; 191(7):1826-1835.
    View in: PubMed
    Score: 0.043
  4. PSTPIP1-associated myeloid-related proteinemia inflammatory syndrome: A rare cause of childhood neutropenia associated with systemic inflammation and hyperzincemia. Pediatr Blood Cancer. 2019 01; 66(1):e27439.
    View in: PubMed
    Score: 0.031
  5. Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN. Blood. 2018 08 09; 132(6):658-662.
    View in: PubMed
    Score: 0.030
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.