← Evidence map

ArticleJournal of human genetics2006

A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association.

M Melin et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

6 papers cite it

2006
2007
2008
2009
2010
2011
2012
2013
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 16946994