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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1981 | 1 |
2000 | 1 |
2005 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 55512
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A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.
Nat Genet. 2005 Aug;37(8):803-5. doi: 10.1038/ng1603. Epub 2005 Jul 17.
Nat Genet. 2005.
PMID: 16025116
Neutral sphingomyelinase 2 (smpd3) in the control of postnatal growth and development.
Stoffel W, Jenke B, Blöck B, Zumbansen M, Koebke J.
Stoffel W, et al.
Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4554-9. doi: 10.1073/pnas.0406380102. Epub 2005 Mar 11.
Proc Natl Acad Sci U S A. 2005.
PMID: 15764706
Free PMC article.
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Cloning and characterization of the mammalian brain-specific, Mg2+-dependent neutral sphingomyelinase.
Hofmann K, Tomiuk S, Wolff G, Stoffel W.
Hofmann K, et al.
Proc Natl Acad Sci U S A. 2000 May 23;97(11):5895-900. doi: 10.1073/pnas.97.11.5895.
Proc Natl Acad Sci U S A. 2000.
PMID: 10823942
Free PMC article.
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Fragilitas ossium: a new autosomal recessive mutation in the mouse.
Guenet JL, Stanescu R, Maroteaux P, Stanescu V.
Guenet JL, et al.
J Hered. 1981 Nov-Dec;72(6):440-1. doi: 10.1093/oxfordjournals.jhered.a109554.
J Hered. 1981.
PMID: 6801109
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