Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3′ MECOM
Lars T. van der Veken,
Merel C. Maiburg,
Floris Groenendaal,
Mariëlle E. van Gijn,
Andries C. Bloem,
Claudia Erpelinck,
Stefan Gröschel,
Mathijs A. Sanders,
Ruud Delwel,
Marc B. Bierings,
Arjan Buijs
Affiliations
Lars T. van der Veken
Department of Genetics, University Medical Center Utrecht, Wilhelmina Children’s Hospital, Utrecht University, Rotterdam, the Netherlands
Merel C. Maiburg
Department of Genetics, University Medical Center Utrecht, Wilhelmina Children’s Hospital, Utrecht University, Rotterdam, the Netherlands
Floris Groenendaal
Department of Neonatology, University Medical Center Utrecht, Wilhelmina Children’s Hospital, Utrecht University, Rotterdam, the Netherlands
Mariëlle E. van Gijn
Department of Genetics, University Medical Center Utrecht, Wilhelmina Children’s Hospital, Utrecht University, Rotterdam, the Netherlands
Andries C. Bloem
Department of Immunology, University Medical Center Utrecht, Wilhelmina Children’s Hospital, Utrecht University, Rotterdam, the Netherlands
Claudia Erpelinck
Department of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands
Stefan Gröschel
Department of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands
Mathijs A. Sanders
Department of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands
Ruud Delwel
Department of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands
Marc B. Bierings
Department of Pediatric Hematology and stem cell transplantation, University Medical Center Utrecht, Wilhelmina Children’s Hospital, Utrecht University, the Netherlands
Arjan Buijs
Department of Genetics, University Medical Center Utrecht, Wilhelmina Children’s Hospital, Utrecht University, Rotterdam, the Netherlands