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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMJ Group 2003
Gaiak:
Original Article
Sarrera elektronikoa: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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