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A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” phenotype

Document Type

Article

Author

Berardinelli, F.; di Masi, A.; Salvatore, M.; Banerjee, S.; Myung, K.; De Villartay, J.P.; Revy, P.; Plebani, A.; Soresina, A.; Taruscio, D.; Tanzarella, C.; Antoccia, A.

Source

In European Journal of Medical Genetics 2007 50(3):176-187

Subject

Language

ISSN

1769-7212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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