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1999 | 1 |
2000 | 1 |
2024 | 0 |
PubMed for id: 460368
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Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3.
Cytogenet Cell Genet. 2000;88(3-4):259-63. doi: 10.1159/000015533.
Cytogenet Cell Genet. 2000.
PMID: 10828604
Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME).
Vitelli F, Piccini M, Caroli F, Franco B, Malandrini A, Pober B, Jonsson J, Sorrentino V, Renieri A.
Vitelli F, et al.
Genomics. 1999 Feb 1;55(3):335-40. doi: 10.1006/geno.1998.5666.
Genomics. 1999.
PMID: 10049589
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