Chromosome 1q23.3q31.1 deletion associated with decreased newborn screening of T cell receptor rearrangement circles (TRECs).

作者信息

Lee Julia S, Becker Bradley A, Kirby Amelia, Knutsen Alan P

机构信息

Department of Pediatrics, Division of Allergy and Immunology, Saint Louis University School of Medicine, St. Louis, Missouri.

Department of Pediatrics, Division of Medical Genetics, Saint Louis University School of Medicine, St. Louis, Missouri.

出版信息

Ann Allergy Asthma Immunol. 2018 Jul;121(1):125-126. doi: 10.1016/j.anai.2018.04.003. Epub 2018 Apr 10.

DOI:10.1016/j.anai.2018.04.003

PMID:29653236

Abstract

摘要

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引用本文的文献

Case Report: Candidate Genes Associated With Prenatal Ultrasound Anomalies in a Fetus With Prenatally Detected 1q23.3q31.2 Deletion.病例报告：产前检测到1q23.3q31.2缺失的胎儿中与产前超声异常相关的候选基因

Front Genet. 2021 Sep 23;12:696624. doi: 10.3389/fgene.2021.696624. eCollection 2021.

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