phenotypeectrodactyly, prognathism (MMEP) a translocation t(6;13)(q21;q12) and microcephaly, ) is disrupted in a patient with SNX3 Sorting nexin 3 (
Year: 2008
Type: article
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2322766173
