{"title":"更正 \"两例具有复杂表型的单亲多条染色体切除术\"。","authors":"","doi":"10.1002/ajmg.a.63837","DOIUrl":null,"url":null,"abstract":"<p>Polonis, K., Lopes, J. L., Cabral, H., Babcock, H. E., Kline, L., Ruiz, K. M., Schwartz, S., Grant, C. L., Hasadsri, L., Rowsey, R. A., & Hoppman, N. L. (2023). Uniparental disomy of multiple chromosomes in two cases with a complex phenotype. American Journal of Medical Genetics Part A, 191A: 1978–1983. https://doi.org/10.1002/ajmg.a.63224</p><p>In the originally published article, Christina L. Grant was inadvertently omitted from the author list. The correct author list is:</p><p>Katarzyna Polonis,<sup>1</sup> Jaime L. Lopes,<sup>2</sup> Huong Cabral,<sup>1</sup> Holly E. Babcock,<sup>3</sup> Laura Kline,<sup>4</sup> Kaylee M. Ruiz,<sup>5</sup> Stuart Schwartz,<sup>4</sup> Christina L. Grant,<sup>6</sup> Linda Hasadsri,<sup>1</sup> Ross A. Rowsey,<sup>1</sup> Nicole L. Hoppman<sup>1</sup></p><p><sup>1</sup>Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA</p><p><sup>2</sup>Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA</p><p><sup>3</sup>Rare Disease Institute, Children's National Hospital, Washington, DC, USA</p><p><sup>4</sup>Women's Health and Genetics, Laboratory Corporation of America, Burlington, North Carolina, USA</p><p><sup>5</sup>Valley Children's Healthcare, Madera, California, USA</p><p><sup>6</sup>Division of Genetics and Metabolism, Children's National Hospital, Washington, DC, USA</p><p>This has been updated in the online version of the article.</p><p>We apologize for this error.</p>","PeriodicalId":7507,"journal":{"name":"American Journal of Medical Genetics Part A","volume":"194 12","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajmg.a.63837","citationCount":"0","resultStr":"{\"title\":\"Correction to “Uniparental disomy of multiple chromosomes in two cases with a complex phenotype”\",\"authors\":\"\",\"doi\":\"10.1002/ajmg.a.63837\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Polonis, K., Lopes, J. L., Cabral, H., Babcock, H. E., Kline, L., Ruiz, K. M., Schwartz, S., Grant, C. L., Hasadsri, L., Rowsey, R. A., & Hoppman, N. L. (2023). Uniparental disomy of multiple chromosomes in two cases with a complex phenotype. American Journal of Medical Genetics Part A, 191A: 1978–1983. https://doi.org/10.1002/ajmg.a.63224</p><p>In the originally published article, Christina L. Grant was inadvertently omitted from the author list. The correct author list is:</p><p>Katarzyna Polonis,<sup>1</sup> Jaime L. Lopes,<sup>2</sup> Huong Cabral,<sup>1</sup> Holly E. Babcock,<sup>3</sup> Laura Kline,<sup>4</sup> Kaylee M. Ruiz,<sup>5</sup> Stuart Schwartz,<sup>4</sup> Christina L. Grant,<sup>6</sup> Linda Hasadsri,<sup>1</sup> Ross A. Rowsey,<sup>1</sup> Nicole L. Hoppman<sup>1</sup></p><p><sup>1</sup>Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA</p><p><sup>2</sup>Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA</p><p><sup>3</sup>Rare Disease Institute, Children's National Hospital, Washington, DC, USA</p><p><sup>4</sup>Women's Health and Genetics, Laboratory Corporation of America, Burlington, North Carolina, USA</p><p><sup>5</sup>Valley Children's Healthcare, Madera, California, USA</p><p><sup>6</sup>Division of Genetics and Metabolism, Children's National Hospital, Washington, DC, USA</p><p>This has been updated in the online version of the article.</p><p>We apologize for this error.</p>\",\"PeriodicalId\":7507,\"journal\":{\"name\":\"American Journal of Medical Genetics Part A\",\"volume\":\"194 12\",\"pages\":\"\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajmg.a.63837\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Medical Genetics Part A\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.63837\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Medical Genetics Part A","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.63837","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
摘要
Polonis, K., Lopes, J. L., Cabral, H., Babcock, H. E., Kline, L., Ruiz, K. M., Schwartz, S., Grant, C. L., Hasadsri, L., Rowsey, R. A., & Hoppman, N. L. (2023)。两例复杂表型的单亲多染色体断裂。美国医学遗传学杂志 A 部分，191A：1978-1983。https://doi.org/10.1002/ajmg.a.63224In，在最初发表的文章中，克里斯蒂娜-格兰特（Christina L. Grant）不慎从作者名单中遗漏。正确的作者名单为：Katarzyna Polonis、1 Jaime L. Lopes、2 Huong Cabral、1 Holly E. Babcock、3 Laura Kline、4 Kaylee M. Ruiz、5 Stuart Schwartz、4 Christina L. Grant、6 Linda Hasadsri、1 Ross A. Rowsey、1 Nicole L. Hoppman11。Hoppman11美国明尼苏达州罗切斯特梅奥诊所检验医学和病理学部2美国俄亥俄州辛辛那提辛辛那提儿童医院医学中心儿科部3美国华盛顿特区国家儿童医院罕见病研究所4妇女健康和遗传学、美国北卡罗来纳州伯灵顿美国实验室公司5美国加利福尼亚州马德拉山谷儿童医疗保健6美国华盛顿特区国立儿童医院遗传学和新陈代谢部这篇文章的在线版本已经更新。我们对此错误深表歉意。
Correction to “Uniparental disomy of multiple chromosomes in two cases with a complex phenotype”
Polonis, K., Lopes, J. L., Cabral, H., Babcock, H. E., Kline, L., Ruiz, K. M., Schwartz, S., Grant, C. L., Hasadsri, L., Rowsey, R. A., & Hoppman, N. L. (2023). Uniparental disomy of multiple chromosomes in two cases with a complex phenotype. American Journal of Medical Genetics Part A, 191A: 1978–1983. https://doi.org/10.1002/ajmg.a.63224
In the originally published article, Christina L. Grant was inadvertently omitted from the author list. The correct author list is:
Katarzyna Polonis,1 Jaime L. Lopes,2 Huong Cabral,1 Holly E. Babcock,3 Laura Kline,4 Kaylee M. Ruiz,5 Stuart Schwartz,4 Christina L. Grant,6 Linda Hasadsri,1 Ross A. Rowsey,1 Nicole L. Hoppman1
1Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA
2Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA
3Rare Disease Institute, Children's National Hospital, Washington, DC, USA
4Women's Health and Genetics, Laboratory Corporation of America, Burlington, North Carolina, USA
5Valley Children's Healthcare, Madera, California, USA
6Division of Genetics and Metabolism, Children's National Hospital, Washington, DC, USA
This has been updated in the online version of the article.
期刊介绍：
The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts:
Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders.
Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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