PAWEL STANKIEWICZ to Chromosomes, Human, Pair 19
This is a "connection" page, showing publications PAWEL STANKIEWICZ has written about Chromosomes, Human, Pair 19.
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Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis. Am J Med Genet A. 2013 Dec; 161A(12):2953-63.
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Periaxin mutations cause recessive Dejerine-Sottas neuropathy. Am J Hum Genet. 2001 Feb; 68(2):325-33.
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