Literature DB >> 7096665

Dyskeratosis congenita: an autosomal dominant disorder.

P K Tchou, T Kohn.   

Abstract

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Year:  1982        PMID: 7096665     DOI: 10.1016/s0190-9622(82)80100-x

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


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  5 in total

1.  Dyskeratosis congenita (Zinsser-Engman-Cole syndrome).

Authors:  S Ganguly
Journal:  Indian J Pediatr       Date:  1996 Nov-Dec       Impact factor: 1.967

2.  T cell immunodeficiency in dyskeratosis congenita.

Authors:  B W Lee; H K Yap; T C Quah; A Chong; C C Seah
Journal:  Arch Dis Child       Date:  1992-04       Impact factor: 3.791

3.  Dyskeratosis congenita.

Authors:  H R Davidson; J M Connor
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

4.  Gastrointestinal involvement in a woman with dyskeratosis congenita.

Authors:  K E Brown; T E Kelly; B M Myers
Journal:  Dig Dis Sci       Date:  1993-01       Impact factor: 3.199

5.  Dyskeratosis Congenita with Portal Hypertension and Oesophageal Webs: A Case Report.

Authors:  Sandeep Khuraiya; Ramesh Raidas; Vinod Jain; Dilip Kachhwaha
Journal:  Indian J Dermatol       Date:  2021 Mar-Apr       Impact factor: 1.494

  5 in total

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