MUSTAFA OZEN to Child
This is a "connection" page, showing publications MUSTAFA OZEN has written about Child.
Connection Strength
0.144
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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.
Score: 0.038
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Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis. Hum Mol Genet. 2015 Oct 01; 24(19):5378-87.
Score: 0.030
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Whole-exome sequencing revealed two novel mutations in Usher syndrome. Gene. 2015 Jun 01; 563(2):215-8.
Score: 0.029
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MicroRNA profiling in lymphocytes and serum of tyrosinemia type-I patients. Mol Biol Rep. 2013 Jul; 40(7):4619-23.
Score: 0.026
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The altered promoter methylation of oxytocin receptor gene in autism. J Neurogenet. 2016 Sep - Dec; 30(3-4):280-284.
Score: 0.008
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Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. Orphanet J Rare Dis. 2015 Sep 30; 10:128.
Score: 0.008
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Characterization of cancer stem-like cells in chordoma. J Neurosurg. 2012 Apr; 116(4):810-20.
Score: 0.006