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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
Open Access status: closed
OpenAlex ID: W2322766173
FWCI:
Cites: 41
Cited by:
Related to: 10