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Year | Number of Results |
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2007 | 1 |
2010 | 1 |
2013 | 1 |
2024 | 0 |
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TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.
Am J Hum Genet. 2013 Aug 8;93(2):197-210. doi: 10.1016/j.ajhg.2013.05.027. Epub 2013 Jun 27.
Am J Hum Genet. 2013.
PMID: 23810381
Free PMC article.
HERV-mediated genomic rearrangement of EYA1 in an individual with branchio-oto-renal syndrome.
Sanchez-Valle A, Wang X, Potocki L, Xia Z, Kang SH, Carlin ME, Michel D, Williams P, Cabrera-Meza G, Brundage EK, Eifert AL, Stankiewicz P, Cheung SW, Lalani SR.
Sanchez-Valle A, et al. Among authors: eifert al.
Am J Med Genet A. 2010 Nov;152A(11):2854-60. doi: 10.1002/ajmg.a.33686.
Am J Med Genet A. 2010.
PMID: 20979191
Free PMC article.
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Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.
Potocki L, Bi W, Treadwell-Deering D, Carvalho CM, Eifert A, Friedman EM, Glaze D, Krull K, Lee JA, Lewis RA, Mendoza-Londono R, Robbins-Furman P, Shaw C, Shi X, Weissenberger G, Withers M, Yatsenko SA, Zackai EH, Stankiewicz P, Lupski JR.
Potocki L, et al. Among authors: eifert a.
Am J Hum Genet. 2007 Apr;80(4):633-49. doi: 10.1086/512864. Epub 2007 Feb 26.
Am J Hum Genet. 2007.
PMID: 17357070
Free PMC article.
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