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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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2003 | 1 |
2011 | 1 |
2015 | 1 |
2024 | 0 |
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Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.
J Med Genet. 2003 Jun;40(6):399-407. doi: 10.1136/jmg.40.6.399.
J Med Genet. 2003.
PMID: 12807959
Free PMC article.
Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.
Kamamoto M, Machida J, Yamaguchi S, Kimura M, Ono T, Jezewski PA, Higashi Y, Nakayama A, Shimozato K, Tokita Y.
Kamamoto M, et al.
Eur J Hum Genet. 2011 Aug;19(8):844-50. doi: 10.1038/ejhg.2011.47. Epub 2011 Mar 30.
Eur J Hum Genet. 2011.
PMID: 21448236
Free PMC article.
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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.
Richards S, et al.
Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.
Genet Med. 2015.
PMID: 25741868
Free PMC article.
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