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Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.
Bittel DC, Yu S, Newkirk H, Kibiryeva N, Holt A 3rd, Butler MG, Cooley LD. Bittel DC, et al. Among authors: butler mg. Cytogenet Genome Res. 2009;124(2):113-20. doi: 10.1159/000207515. Epub 2009 May 5. Cytogenet Genome Res. 2009. PMID: 19420922 Free PMC article.
ANKRD11 gene deletion in a 17-year-old male.
Youngs EL, Hellings JA, Butler MG. Youngs EL, et al. Among authors: butler mg. Clin Dysmorphol. 2011 Jul;20(3):170-171. doi: 10.1097/MCD.0b013e328346f6ae. Clin Dysmorphol. 2011. PMID: 21527850 Free PMC article. No abstract available.
The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Cox DM, Butler MG. Cox DM, et al. Among authors: butler mg. Int J Mol Sci. 2015 Feb 13;16(2):4068-82. doi: 10.3390/ijms16024068. Int J Mol Sci. 2015. PMID: 25689425 Free PMC article. Review.
Growth Charts for Prader-Willi Syndrome During Growth Hormone Treatment.
Butler MG, Lee J, Cox DM, Manzardo AM, Gold JA, Miller JL, Roof E, Dykens E, Kimonis V, Driscoll DJ. Butler MG, et al. Clin Pediatr (Phila). 2016 Sep;55(10):957-74. doi: 10.1177/0009922815617973. Epub 2016 Feb 3. Clin Pediatr (Phila). 2016. PMID: 26842920 Free PMC article.
516 results