Dyskeratosis Congenita
Author:
Publisher
Springer Vienna
Link
http://link.springer.com/content/pdf/10.1007/978-3-211-69500-5_44
Reference62 articles.
1. Aalfs CM, van denBerg H, Barth PG, Hennekam RC (1995) The Hoyeraal-Hreidarsson syndrome: the fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasia. Eur J Pediatr 154: 304–308.
2. Akaboshi S, Yoshimura M, Hara T, Kageyama H, Nishikwa K, Kawakami T, Ieshima A, Takeshita K(2000) A case of Hoyeraal-Hreidarsson syndrome: delayed myelination and hypoplasia of corpus callosum are other important signs. Neuropediatrics 31: 141–144.
3. Arca E, Tuzun A, Tastan HB, Akar A, Kose O (2003) Dyskeratosis congenita with esophageal and anal stricture. Int J Dermatol 42: 555–557.
4. Auerbach AD (1995) Fanconi anemia. Dermatol Clin 13: 41–49.
5. Bessler M, Wilson DB, Mason PJ (2004) Dyskeratosis congenital and telomerase. Curr Opin Pediatr 16: 23–28.
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