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Year | Number of Results |
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2018 | 1 |
2021 | 2 |
2022 | 1 |
2024 | 0 |
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Paternal retraction of a fragile X allele to normal size, showing normal function over two generations.
Am J Med Genet A. 2022 Jan;188(1):304-309. doi: 10.1002/ajmg.a.62500. Epub 2021 Sep 21.
Am J Med Genet A. 2022.
PMID: 34545686
Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.
Jarmolowicz AI, Baker EK, Bartlett E, Francis D, Ling L, Gamage D, Delatycki MB, Godler DE.
Jarmolowicz AI, et al. Among authors: bartlett e.
Am J Med Genet A. 2021 May;185(5):1498-1503. doi: 10.1002/ajmg.a.62106. Epub 2021 Feb 5.
Am J Med Genet A. 2021.
PMID: 33544979
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Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete Retraction.
Prawer Y, Hunter M, Cronin S, Ling L, Aliaga Vera S, Fahey M, Gelfand N, Oertel R, Bartlett E, Francis D, Godler D.
Prawer Y, et al. Among authors: bartlett e.
Genes (Basel). 2018 Jun 7;9(6):287. doi: 10.3390/genes9060287.
Genes (Basel). 2018.
PMID: 29880767
Free PMC article.
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