A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

Sagittal craniosynostosis is the most common form of craniosynostosis, affecting approximately one in 5,000 newborns. We conducted, to our knowledge, the first genome-wide association study for nonsyndromic sagittal craniosynostosis (sNSC) using 130 non-Hispanic case-parent trios of European ancestr...

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Xehetasun bibliografikoak
Egile Nagusiak: Justice, C, Yagnik, G, Kim, Y, Peter, I, Jabs, E, Erazo, M, Ye, X, Ainehsazan, E, Shi, L, Cunningham, M, Kimonis, V, Roscioli, T, Wall, SA, Wilkie, A, Stoler, J, Richtsmeier, J, Heuzé, Y, Sanchez-Lara, P, Buckley, M, Druschel, C, Mills, J, Caggana, M, Romitti, P, Kay, D, Senders, C
Formatua: Journal article
Hizkuntza:English
Argitaratua: 2012