Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

MSX1 has been proposed as a gene in which mutations may contribute to non-syndromic forms of cleft lip and/or cleft palate. Support for this comes from human linkage and linkage disequilibrium studies, chromosomal deletions resulting in haploinsufficiency, a large family with a stop codon mutation t...

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書誌詳細
主要な著者: Jezewski, P, Vieira, A, Nishimura, C, Ludwig, B, Johnson, M, O'Brien, S, Daack-Hirsch, S, Schultz, R, Weber, A, Nepomucena, B, Romitti, P, Christensen, K, Orioli, I, Castilla, E, Machida, J, Natsume, N, Murray, J
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Group 2003
主題:
Original Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735501/
https://ncbi.nlm.nih.gov/pubmed/12807959
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.6.399
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