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

doi:10.1016/j.pedneo.2021.11.004

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

^*この論文の責任著者

周産母子センター

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

本文言語	英語
ページ（範囲）	298-300
ページ数	3
ジャーナル	Pediatrics and Neonatology
巻	63
号	3
DOI	https://doi.org/10.1016/j.pedneo.2021.11.004
出版ステータス	出版済み - 2022/05

ASJC Scopus 主題領域

小児科学、周産期医学および子どもの健康

文献へのアクセス

10.1016/j.pedneo.2021.11.004

引用スタイル

@article{0ba17387056640718bf145dfb404d422,

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

author = "Kentaro Tamura and Tomonari Awaya and Takahito Wada and Tatsuya Fujii and Taketoshi Yoshida",

note = "Funding Information: The authors thank Dr Yasuhiro Yamashiro, Division of Clinical Laboratory Science, Yamaguchi University for a quantitative analysis of α-globin genes for case 1.",

year = "2022",

month = may,

doi = "10.1016/j.pedneo.2021.11.004",

language = "英語",

volume = "63",

pages = "298--300",

journal = "Pediatrics and Neonatology",

issn = "1875-9572",

publisher = "Elsevier (Singapore) Pte Ltd",

number = "3",

}

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 その他.
In: Pediatrics and Neonatology, Vol. 63, No. 3, 05.2022, p. 298-300.

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

TY - JOUR

T1 - Noniron deficiency microcytic anemia, dysmorphic features, and intellectual disability

T2 - Diagnostic clues for α-thalassemia/mental retardation associated with chromosome 16 syndrome

AU - Tamura, Kentaro

AU - Awaya, Tomonari

AU - Wada, Takahito

AU - Fujii, Tatsuya

AU - Yoshida, Taketoshi

N1 - Funding Information: The authors thank Dr Yasuhiro Yamashiro, Division of Clinical Laboratory Science, Yamaguchi University for a quantitative analysis of α-globin genes for case 1.

PY - 2022/5

Y1 - 2022/5

UR - http://www.scopus.com/inward/record.url?scp=85125676491&partnerID=8YFLogxK

U2 - 10.1016/j.pedneo.2021.11.004

DO - 10.1016/j.pedneo.2021.11.004

M3 - 学術論文

C2 - 35246371

AN - SCOPUS:85125676491

SN - 1875-9572

VL - 63

SP - 298

EP - 300

JO - Pediatrics and Neonatology

JF - Pediatrics and Neonatology

IS - 3

ER -