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searching for OPHN1 2 found (7 total)

alternate case: oPHN1

Ephrin B1 (1,097 words) [view diff] exact match in snippet view article find links to article

R, et al. (December 2007). "Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome". Clin. Genet
STARD8 (816 words) [view diff] exact match in snippet view article find links to article
Zackai E, Wieacker P (Dec 2007). "Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome". Clinical Genetics