A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
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| Description | scientific article published on 21 February 2007 |
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author: Domenica Taruscio Francesco Berardinelli Patrick Revy Jean-Pierre de Villartay |
| Publication date | February 21, 2007 |
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