Seckel Syndrome
Reference38 articles.
1. Abou-zahr, F., Bejjani, B., Kruyt, F. A. E., et al. (1999). Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome. American Journal of Medical Genetics, 83, 388–391. 2. Al-Dosari, M. S., Shaheen, R., Colak, D., et al. (2009). Novel CENPJ mutation causes Seckel syndrome. Journal of Medical Genetics, 47, 411–414. 3. Anderson, C. E., Wallerstein, R., Zamerowski, S. T., et al. (1997). Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome. American Journal of Medical Genetics, 72, 281–285. 4. Arnold, S. R., Spicer, D., Kouseff, B., et al. (1999). Seckel-like syndrome in three siblings. Pediatric and Developmental Pathology, 2, 180–187. 5. Bangstad, H. J., Beck-Nielsen, H., Hother-Neilsen, O., et al. (1989). Primordial bird-headed nanism associated with progressive ataxia, early onset insulin resistant diabetes, goiter, and primary gonadal insufficiency. A new syndrome. Acta Paediatrica Scandinavica, 78, 488–493.
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