Upal Hossain
London, ENG, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
The evolving genetic landscape of telomere biology disorder dyskeratosis congenita.
Journal: EMBO molecular medicine
Published: April 10, 2024
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants.
Journal: Nature communications
Published: February 04, 2019
14-month old boy with abrupt-onset petechiae and bruising.
Journal: Archives of disease in childhood. Education and practice edition
Published: February 01, 2019
Successful pregnancy in the context of previously undiagnosed chronic lymphocytic leukaemia: A case report and literature review.
Journal: Obstetric medicine
Published: November 06, 2016
Better Transition Readiness for Adolescents Begins With Effective Communication.
Journal: Journal of pediatric hematology/oncology
Published: July 25, 2015
ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function.
Journal: American journal of human genetics
Published: November 13, 2013
Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia.
Journal: American journal of human genetics
Published: January 30, 2012
Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia.
Journal: British journal of haematology
Published: January 15, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026