Comment on: Acquired monosomy 7 myelodysplastic syndrome in a child with clinical features of dyskeratosis congenita and IMAGe association
Pediatr Blood Cancer
.
2018 Jan;65(1).
doi: 10.1002/pbc.26747.
Epub 2017 Aug 17.
Authors
David B Wilson
1
,
Monica Bessler
2
3
,
Thomas W Ferkol
1
,
Shalini Shenoy
1
,
Naoko Amano
4
,
Tomohiro Ishii
4
,
Hirohito Shima
5
,
Satoshi Narumi
5
Affiliations
1
Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, Missouri.
2
Department of Pediatrics, University of Pennsylvania, Philadelphia, Pennsylvania.
3
Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
4
Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
5
Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
PMID:
28834235
DOI:
10.1002/pbc.26747
No abstract available
Publication types
Letter
Comment
MeSH terms
Child
Chromosome Deletion
Chromosomes, Human, Pair 7
Dyskeratosis Congenita / genetics*
Humans
Myelodysplastic Syndromes / genetics*
Supplementary concepts
Chromosome 7, monosomy