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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1998 | 2 |
1999 | 2 |
2024 | 0 |
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KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs.
Genomics. 1999 Sep 15;60(3):251-7. doi: 10.1006/geno.1999.5904.
Genomics. 1999.
PMID: 10493825
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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Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?
Jonsson JJ, Renieri A, Gallagher PG, Kashtan CE, Cherniske EM, Bruttini M, Piccini M, Vitelli F, Ballabio A, Pober BR.
Jonsson JJ, et al.
J Med Genet. 1998 Apr;35(4):273-8. doi: 10.1136/jmg.35.4.273.
J Med Genet. 1998.
PMID: 9598718
Free PMC article.
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FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.
Piccini M, Vitelli F, Bruttini M, Pober BR, Jonsson JJ, Villanova M, Zollo M, Borsani G, Ballabio A, Renieri A.
Piccini M, et al.
Genomics. 1998 Feb 1;47(3):350-8. doi: 10.1006/geno.1997.5104.
Genomics. 1998.
PMID: 9480748
Free article.
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