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Contiguous gene deletion of TBX5 and TBX3: report of another case.
Forzano F, Foley PA, Keane MR, Brain CE, Smith GD, Yates RW, Ellershaw D, Calder AD, Scott RH. Forzano F, et al. Among authors: ellershaw d. Clin Dysmorphol. 2018 Jan;27(1):6-8. doi: 10.1097/MCD.0000000000000199. Clin Dysmorphol. 2018. PMID: 28961683 No abstract available.
Stem cell transplantation for tetratricopeptide repeat domain 7A deficiency: long-term follow-up.
Kammermeier J, Lucchini G, Pai SY, Worth A, Rampling D, Amrolia P, Silva J, Chiesa R, Rao K, Noble-Jamieson G, Gasparetto M, Ellershaw D, Uhlig H, Sebire N, Elawad M, Notarangelo L, Shah N, Veys P. Kammermeier J, et al. Among authors: ellershaw d. Blood. 2016 Sep 1;128(9):1306-8. doi: 10.1182/blood-2016-01-696385. Epub 2016 Jul 14. Blood. 2016. PMID: 27418642 Free article. No abstract available.
Trisomy 21 mid-trimester amniotic fluid induced pluripotent stem cells maintain genetic signatures during reprogramming: implications for disease modeling and cryobanking.
Pipino C, Mukherjee S, David AL, Blundell MP, Shaw SW, Sung P, Shangaris P, Waters JJ, Ellershaw D, Cavazzana M, Mostoslavsky G, Pandolfi A, Pierro A, Guillot PV, Thrasher AJ, De Coppi P. Pipino C, et al. Among authors: ellershaw d. Cell Reprogram. 2014 Oct;16(5):331-44. doi: 10.1089/cell.2013.0091. Epub 2014 Aug 27. Cell Reprogram. 2014. PMID: 25162836