Noniron deficiency microcytic anemia, dysmorphic features, and intellectual disability: Diagnostic clues for α-thalassemia/mental retardation associated with chromosome 16 syndrome
Kentaro Tamura,
Tomonari Awaya,
Takahito Wada,
Tatsuya Fujii,
Taketoshi Yoshida
Affiliations
Kentaro Tamura
Division of Neonatology, Maternal and Perinatal Center, Toyama University Hospital, Toyama, Japan; Corresponding author. Division of Neonatology, Maternal and Perinatal Center, Toyama University Hospital, 2630 Sugitani, Toyama, 930-0194, Japan.
Tomonari Awaya
Department of Anatomy and Developmental Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan
Takahito Wada
Department of Medical Ethics and Medical Genetics, Kyoto University Graduate School of Medicine, Kyoto, Japan
Tatsuya Fujii
Department of Pediatrics, Shiga Medical Center for Children, Moriyama, Japan
Taketoshi Yoshida
Division of Neonatology, Maternal and Perinatal Center, Toyama University Hospital, Toyama, Japan