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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2010 | 2 |
2025 | 0 |
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3 results
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A male with unilateral microphthalmia reveals a role for TMX3 in eye development.
PLoS One. 2010 May 11;5(5):e10565. doi: 10.1371/journal.pone.0010565.
PLoS One. 2010.
PMID: 20485507
Free PMC article.
Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRalpha reveals rare variants in diaphragmatic hernia patients.
Bleyl SB, Moshrefi A, Shaw GM, Saijoh Y, Schoenwolf GC, Pennacchio LA, Slavotinek AM.
Bleyl SB, et al.
Eur J Hum Genet. 2007 Sep;15(9):950-8. doi: 10.1038/sj.ejhg.5201872. Epub 2007 Jun 13.
Eur J Hum Genet. 2007.
PMID: 17568391
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A maternally inherited chromosome 18q22.1 deletion in a male with late-presenting diaphragmatic hernia and microphthalmia-evaluation of DSEL as a candidate gene for the diaphragmatic defect.
Zayed H, Chao R, Moshrefi A, Lopezjimenez N, Delaney A, Chen J, Shaw GM, Slavotinek AM.
Zayed H, et al.
Am J Med Genet A. 2010 Apr;152A(4):916-23. doi: 10.1002/ajmg.a.33341.
Am J Med Genet A. 2010.
PMID: 20358601
Free PMC article.
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