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April 27, 2007BloodOpen Access

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita

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BABlanche P. AlterGBGabriela M. BaerlocherSSSharon A. Savage

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Alter et al. (2007) studied this question.

synapsesocial.com/papers/69dd3f717808b00a4799bb2ahttps://doi.org/10.1182/blood-2007-02-075598
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  1. 1Haploinsufficiency of t <i>e</i> lomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita2005 · 456 citations