Rare diseases, common barriers: disparities in pediatric clinical genetics outcomes.

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作者： Monica H,Wojcik ^[1] ; Mairead,Bresnahan ^[2] ; Maya C,Del Rosario ^[3] ; Mayra Martinez,Ojeda ^[4] ; Amy,Kritzer ^[4] ; Yarden S,Fraiman ^[4]

作者单位： Division of Newborn Medicine, Department of Medicine, Boston Children's Hospital, Boston, MA, 02115, USA. monica.wojcik@childrens.harvard.edu. ^[1] Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, MA, 02115, USA. monica.wojcik@childrens.harvard.edu. ^[2] Harvard Medical School, Boston, MA, USA. monica.wojcik@childrens.harvard.edu. ^[3] Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, MA, 02115, USA. ^[4] Harvard Medical School, Boston, MA, USA. ^[5] Division of Newborn Medicine, Department of Medicine, Boston Children's Hospital, Boston, MA, 02115, USA. ^[6] Department of Neonatology, Beth Israel Deaconess Medical Center, Boston, MA, USA. ^[7]

主题词人类(Humans);少见病(Rare Diseases);回顾性研究(Retrospective Studies);转诊和会诊(Referral and Consultation);卫生保健差异(Healthcare Disparities)

DOI 10.1038/s41390-022-02240-3

PMID 35963884

发布时间 2023-02-19

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