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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 1 |
2002 | 1 |
2010 | 1 |
2024 | 0 |
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Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis.
J Neurosci. 2010 Feb 24;30(8):2880-7. doi: 10.1523/JNEUROSCI.4196-09.2010.
J Neurosci. 2010.
PMID: 20181585
Free PMC article.
Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome.
Prakash SK, Cormier TA, McCall AE, Garcia JJ, Sierra R, Haupt B, Zoghbi HY, Van Den Veyver IB.
Prakash SK, et al.
Hum Mol Genet. 2002 Dec 1;11(25):3237-48. doi: 10.1093/hmg/11.25.3237.
Hum Mol Genet. 2002.
PMID: 12444108
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A short pseudoautosomal region in laboratory mice.
Perry J, Palmer S, Gabriel A, Ashworth A.
Perry J, et al.
Genome Res. 2001 Nov;11(11):1826-32. doi: 10.1101/gr.203001.
Genome Res. 2001.
PMID: 11691846
Free PMC article.
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