Connection

MUSTAFA OZEN to Child

This is a "connection" page, showing publications MUSTAFA OZEN has written about Child.
Connection Strength

0.144
  1. Revealing the functions of novel mutations in RAB3GAP1 in Martsolf and Warburg micro syndromes. Am J Med Genet A. 2019 04; 179(4):579-587.
    View in: PubMed
    Score: 0.038
  2. Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis. Hum Mol Genet. 2015 Oct 01; 24(19):5378-87.
    View in: PubMed
    Score: 0.030
  3. Whole-exome sequencing revealed two novel mutations in Usher syndrome. Gene. 2015 Jun 01; 563(2):215-8.
    View in: PubMed
    Score: 0.029
  4. MicroRNA profiling in lymphocytes and serum of tyrosinemia type-I patients. Mol Biol Rep. 2013 Jul; 40(7):4619-23.
    View in: PubMed
    Score: 0.026
  5. The altered promoter methylation of oxytocin receptor gene in autism. J Neurogenet. 2016 Sep - Dec; 30(3-4):280-284.
    View in: PubMed
    Score: 0.008
  6. Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. Orphanet J Rare Dis. 2015 Sep 30; 10:128.
    View in: PubMed
    Score: 0.008
  7. Characterization of cancer stem-like cells in chordoma. J Neurosurg. 2012 Apr; 116(4):810-20.
    View in: PubMed
    Score: 0.006
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.