Literature DB >> 14312691

THE ASSOCIATION OF DYSKERATOSIS CONGENITA AND FANCONI'S ANAEMIA.

M ADDISON, M S RICE.   

Abstract

Entities:  

Keywords:  ANEMIA; DIAGNOSIS, DIFFERENTIAL; ESOPHAGEAL STENOSIS; FANCONI SYNDROME; GENETICS; PIGMENTATION DISORDERS; POIKILODERMA CONGENITALE; SKIN DISEASES

Mesh：

Year:  1965        PMID： 14312691

Source DB:  PubMed          Journal:  Med J Aust        ISSN： 0025-729X            Impact factor:   7.738


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  6 in total

1.  Inactivation of the tumor suppressor genes causing the hereditary syndromes predisposing to head and neck cancer via promoter hypermethylation in sporadic head and neck cancers.

Authors:  Ian M Smith; Suhail K Mithani; Wojciech K Mydlarz; Steven S Chang; Joseph A Califano
Journal:  ORL J Otorhinolaryngol Relat Spec       Date:  2010-03-24       Impact factor: 1.538

2.  The gastrointestinal manifestations of telomere-mediated disease.

Authors:  Naudia L Jonassaint; Nini Guo; Joseph A Califano; Elizabeth A Montgomery; Mary Armanios
Journal:  Aging Cell       Date:  2013-01-04       Impact factor: 9.304

Review 3.  Cancer in dyskeratosis congenita.

Authors:  Blanche P Alter; Neelam Giri; Sharon A Savage; Philip S Rosenberg
Journal:  Blood       Date:  2009-03-12       Impact factor: 22.113

4.  The cell cycle of lymphocytes in Fanconi anemia.

Authors:  B Dutrillaux; A Aurias; A M Dutrillaux; D Buriot; M Prieur
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 5.  Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature.

Authors:  C Sirinavin; A A Trowbridge
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

6.  Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblasts.

Authors:  D M DeBauche; G S Pai; W S Stanley
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025
  6 in total

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