{"title":"16号染色体孤本二体导致的Hb Bart病:只有一方携带α0-地中海贫血的妊娠胎儿需要临床警惕。","authors":"Xing-Mei Xie, Fan Jiang, Qiu-Xia Yu, Dong-Zhi Li","doi":"10.1080/03630269.2025.2556722","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":12997,"journal":{"name":"Hemoglobin","volume":" ","pages":"1-3"},"PeriodicalIF":1.0000,"publicationDate":"2025-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hb Bart's Disease Due to Uniparental Disomy for Chromosome 16: The Need for Clinical Vigilance in Hydropic Fetuses with Only One Parent Carrying α<sup>0</sup>-Thalassemia.\",\"authors\":\"Xing-Mei Xie, Fan Jiang, Qiu-Xia Yu, Dong-Zhi Li\",\"doi\":\"10.1080/03630269.2025.2556722\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":12997,\"journal\":{\"name\":\"Hemoglobin\",\"volume\":\" \",\"pages\":\"1-3\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2025-09-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Hemoglobin\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/03630269.2025.2556722\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hemoglobin","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/03630269.2025.2556722","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Hb Bart's Disease Due to Uniparental Disomy for Chromosome 16: The Need for Clinical Vigilance in Hydropic Fetuses with Only One Parent Carrying α0-Thalassemia.
期刊介绍:
Hemoglobin is a journal in the English language for the communication of research and information concerning hemoglobin in humans and other species. Hemoglobin publishes articles, reviews, points of view
The journal covers topics such as:
structure, function, genetics and evolution of hemoglobins
biochemical and biophysical properties of hemoglobin molecules
characterization of hemoglobin disorders (variants and thalassemias),
consequences and treatment of hemoglobin disorders
epidemiology and prevention of hemoglobin disorders (neo-natal and adult screening)
modulating factors
methodology used for diagnosis of hemoglobin disorders