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Year | Number of Results |
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1993 | 1 |
1998 | 1 |
2002 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 8724
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Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype.
J Med Genet. 2002 Dec;39(12):893-9. doi: 10.1136/jmg.39.12.893.
J Med Genet. 2002.
PMID: 12471201
Free PMC article.
Identification of a family of sorting nexin molecules and characterization of their association with receptors.
Haft CR, de la Luz Sierra M, Barr VA, Haft DH, Taylor SI.
Haft CR, et al.
Mol Cell Biol. 1998 Dec;18(12):7278-87. doi: 10.1128/MCB.18.12.7278.
Mol Cell Biol. 1998.
PMID: 9819414
Free PMC article.
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Split-foot anomaly, microphthalmia, cleft-lip and cleft-palate, and mental retardation associated with a chromosome 6;13 translocation.
Viljoen DL, Smart R.
Viljoen DL, et al.
Clin Dysmorphol. 1993 Jul;2(3):274-7.
Clin Dysmorphol. 1993.
PMID: 8287191
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