Novel Mutation in the DKC1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome As a Rare Differential Diagnosis in Pontocerebellar Hypoplasia, Primary Microcephaly, and Progressive Bone Marrow Failure.
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| Description | scientific article published on 7 March 2016 |
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author: Gabriele Hahn Meinolf Suttorp Nataliya Di Donato Maja von der Hagen |
| Publication date | March 7, 2016 |
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