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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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2000 | 1 |
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2024 | 0 |
PubMed (OMIM) for id: 23187
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Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes.
J Med Genet. 2023 Aug;60(8):819-826. doi: 10.1136/jmg-2022-108763. Epub 2022 Dec 21.
J Med Genet. 2023.
PMID: 36543534
Identification and characterization of human LL5A gene and mouse Ll5a gene in silico.
Katoh M, Katoh M.
Katoh M, et al.
Int J Oncol. 2003 Nov;23(5):1477-83.
Int J Oncol. 2003.
PMID: 14532993
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Identification of pleckstrin-homology-domain-containing proteins with novel phosphoinositide-binding specificities.
Dowler S, Currie RA, Campbell DG, Deak M, Kular G, Downes CP, Alessi DR.
Dowler S, et al.
Biochem J. 2000 Oct 1;351(Pt 1):19-31. doi: 10.1042/0264-6021:3510019.
Biochem J. 2000.
PMID: 11001876
Free PMC article.
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Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.
Ishikawa K, Nagase T, Suyama M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O.
Ishikawa K, et al.
DNA Res. 1998 Jun 30;5(3):169-76. doi: 10.1093/dnares/5.3.169.
DNA Res. 1998.
PMID: 9734811
Free article.
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