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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Detaylı Bibliyografya
Asıl Yazarlar:	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
Materyal Türü:	Journal article
Dil:	English
Baskı/Yayın Bilgisi:	2012

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

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