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2009 1
2010 3
2012 1
2022 0
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Page 1
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Solomon BD, Lacbawan F, Mercier S, Clegg NJ, Delgado MR, Rosenbaum K, Dubourg C, David V, Olney AH, Wehner LE, Hehr U, Bale S, Paulussen A, Smeets HJ, Hardisty E, Tylki-Szymanska A, Pronicka E, Clemens M, McPherson E, Hennekam RC, Hahn J, Stashinko E, Levey E, Wieczorek D, Roeder E, Schell-Apacik CC, Booth CW, Thomas RL, Kenwrick S, Cummings DA, Bous SM, Keaton A, Balog JZ, Hadley D, Zhou N, Long R, Vélez JI, Pineda-Alvarez DE, Odent S, Roessler E, Muenke M. Solomon BD, et al. Among authors: bous sm. J Med Genet. 2010 Aug;47(8):513-24. doi: 10.1136/jmg.2009.073049. Epub 2009 Dec 2. J Med Genet. 2010. PMID: 19955556 Free PMC article.
Consideration of VACTERL association in patients with trisomy 21.
Solomon BD, Bous SM, Bianconi S, Pineda-Alvarez DE. Solomon BD, et al. Among authors: bous sm. Clin Dysmorphol. 2010 Oct;19(4):209-211. doi: 10.1097/MCD.0b013e32833b2b9c. Clin Dysmorphol. 2010. PMID: 20512033 Free PMC article. No abstract available.