Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype (Q24672616)
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(P31) (Q13442814)
(P304) 893-9
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(P478) 39
(P577) +2002-12-00T00:00:00Z
(P921) (Q431643)
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(P1476) "Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype" (language: en)
(P2093) V S Vervoort
D Viljoen
R Smart
G Suthers
B R DuPont
A Abbott
C E Schwartz
(P2860) (Q24679311)
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