ArticleJournal of medical genetics2002

Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype.

V S Vervoort et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.