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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2015 | 2 |
2016 | 1 |
2024 | 0 |
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BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations.
J Clin Invest. 2015 Jun;125(6):2363-8. doi: 10.1172/JCI81163. Epub 2015 May 4.
J Clin Invest. 2015.
PMID: 25938782
Free PMC article.
Clinical Trial.
Brain malformations in a patient with deletion 2p16.1: A refinement of the phenotype to BCL11A.
Balci TB, Sawyer SL, Davila J, Humphreys P, Dyment DA.
Balci TB, et al.
Eur J Med Genet. 2015 Jun-Jul;58(6-7):351-4. doi: 10.1016/j.ejmg.2015.04.006. Epub 2015 May 13.
Eur J Med Genet. 2015.
PMID: 25979662
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BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
Dias C, Estruch SB, Graham SA, McRae J, Sawiak SJ, Hurst JA, Joss SK, Holder SE, Morton JE, Turner C, Thevenon J, Mellul K, Sánchez-Andrade G, Ibarra-Soria X, Deriziotis P, Santos RF, Lee SC, Faivre L, Kleefstra T, Liu P, Hurles ME; DDD Study; Fisher SE, Logan DW.
Dias C, et al.
Am J Hum Genet. 2016 Aug 4;99(2):253-74. doi: 10.1016/j.ajhg.2016.05.030. Epub 2016 Jul 21.
Am J Hum Genet. 2016.
PMID: 27453576
Free PMC article.
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