Noniron deficiency microcytic anemia, dysmorphic features, and intellectual disability: Diagnostic clues for &#945;-thalassemia/mental retardation associated with chromosome 16 syndrome.

Tamura, Kentaro; Awaya, Tomonari; Wada, Takahito; Fujii, Tatsuya; Yoshida, Taketoshi

Noniron deficiency microcytic anemia, dysmorphic features, and intellectual disability: Diagnostic clues for α-thalassemia/mental retardation associated with chromosome 16 syndrome.

Tamura, Kentaro; Awaya, Tomonari; Wada, Takahito; Fujii, Tatsuya; Yoshida, Taketoshi.

Affiliation

Tamura K; Division of Neonatology, Maternal and Perinatal Center, Toyama University Hospital, Toyama, Japan. Electronic address: tamura@med.u-toyama.ac.jp.
Awaya T; Department of Anatomy and Developmental Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Wada T; Department of Medical Ethics and Medical Genetics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Fujii T; Department of Pediatrics, Shiga Medical Center for Children, Moriyama, Japan.
Yoshida T; Division of Neonatology, Maternal and Perinatal Center, Toyama University Hospital, Toyama, Japan.

Pediatr Neonatol ; 63(3): 298-300, 2022 05.

Article in En | MEDLINE | ID: mdl-35246371

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alpha-Thalassemia / Anemia, Hypochromic / Intellectual Disability Type of study: Diagnostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Pediatr Neonatol Year: 2022 Document type: Article

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