The Role of Genetic Testing in Hereditary Poikiloderma: A Case Report
Saved in:
Main Authors: | Sarah El-Heis MBBS (Author), Keith M. Godfrey BM, PhD, FRCP (Author) |
---|---|
Format: | Book |
Published: |
SAGE Publishing,
2017-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
by: Raphaëlle Goussot, MD, et al.
Published: (2017) -
Poikiloderma of Civatte
by: Uladzimir P. Adaskevich, et al.
Published: (2013) -
Mutation in FAM111B Causes Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary Fibrosis
by: Fuying Chen, et al.
Published: (2019) -
Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis: Hepatic disease in a child with a novel pathogenic variant of FAM111B
by: Yelena Dokic, BSA, et al.
Published: (2020) -
comment: Poikiloderma of Civatte
by: Anca Chiriac, et al.
Published: (2013)