The gastrointestinal manifestations of telomere-mediated disease

The telomere syndromes

(2012) Mary Armanios et al.   NATURE REVIEWS GENETICS

Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase

(2011) E. M. Parry et al.   BLOOD

Three novel truncating TINF2 mutations causing severe dyskeratosis congenita in early childhood

(2011) GS Sasa et al.   CLINICAL GENETICS

Dyskeratosis congenita: a combined immunodeficiency with broad clinical spectrum - a single-center pediatric experience

(2011) S. Jyonouchi et al.   PEDIATRIC ALLERGY AND IMMUNOLOGY

Tissue-Resident Adult Stem Cell Populations of Rapidly Self-Renewing Organs

(2010) Nick Barker et al.   Cell Stem Cell

Cytogenetic studies of skin fibroblast cultures from a karyotypically normal female with dyskeratosis congenita

(2010) Hildegard Kehrer et al.   CLINICAL GENETICS

Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal-Hreidarsson syndrome

(2010) F. Touzot et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Short Telomeres are Sufficient to Cause the Degenerative Defects Associated with Aging

(2009) Mary Armanios et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Syndromes of Telomere Shortening

(2009) Mary Armanios   Annual Review of Genomics and Human Genetics

Cancer in dyskeratosis congenita

(2009) B. P. Alter et al.   BLOOD

Dyskeratosis Congenita

(2009) Sharon A. Savage et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

Severe Variant of X-linked Dyskeratosis Congenita (Hoyeraal-Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy

(2009) Ingo Borggraefe et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION