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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 1 |
2001 | 1 |
2005 | 2 |
2006 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 1393545
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Deletion of PREPL, a gene encoding a putative serine oligopeptidase, in patients with hypotonia-cystinuria syndrome.
Am J Hum Genet. 2006 Jan;78(1):38-51. doi: 10.1086/498852. Epub 2005 Nov 23.
Am J Hum Genet. 2006.
PMID: 16385448
Free PMC article.
The 2p21 deletion syndrome: characterization of the transcription content.
Parvari R, Gonen Y, Alshafee I, Buriakovsky S, Regev K, Hershkovitz E.
Parvari R, et al.
Genomics. 2005 Aug;86(2):195-211. doi: 10.1016/j.ygeno.2005.04.001.
Genomics. 2005.
PMID: 15913950
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A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
Parvari R, Brodyansky I, Elpeleg O, Moses S, Landau D, Hershkovitz E.
Parvari R, et al.
Am J Hum Genet. 2001 Oct;69(4):869-75. doi: 10.1086/323624. Epub 2001 Aug 24.
Am J Hum Genet. 2001.
PMID: 11524703
Free PMC article.
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Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro.
Ishikawa K, Nagase T, Nakajima D, Seki N, Ohira M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O.
Ishikawa K, et al.
DNA Res. 1997 Oct 31;4(5):307-13. doi: 10.1093/dnares/4.5.307.
DNA Res. 1997.
PMID: 9455477
Free article.
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