학술논문
Mutations in ZIC2 in human holoprosencephaly: Description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals
Document Type
Article
Author
Solomon, B.D.; Lacbawan, F.; Bous, S.M.; Keaton, A.; Balog, J.Z.; Hadley, D.; Zhou, N.; Long, R.; Vélez, J.I.; Pineda-Alvarez, D.E.; Roessler, E.; Muenke, M.; Mercier, S.; Dubourg, C.; David, V.; Odent, S.; Clegg, N.J.; Delgado, M.R.; Rosenbaum, K.; Olney, A.H.; Wehner, L.-E.; Hehr, U.; Bale, S.; Paulussen, A.; Smeets, H.J.; Hardisty, E.; Tylki-Szymanska, A.; Pronicka, E.; Clemens, M.; McPherson, E.; Hennekam, R.C.M.; Hahn, J.; Stashinko, E.; Levey, E.; Wieczorek, D.; Roeder, E.; Schell-Apacik, C.C.; Booth, C.W.; Thomas, R.L.; Kenwrick, S.; Cummings, D.A.T.
Source
In: Journal of Medical Genetics . (Journal of Medical Genetics, August 2010, 47(8):513-524)
Subject
Language
English
ISSN
00222593
14686244
14686244