Cargando…
High-risk phenotypes of genetic disease in a Neonatal Intensive Care Unit population
Autores principales: | Xiao, Tiantian, Ni, Qi, Chen, Huiyao, Wang, Huijun, Yang, Lin, Wu, Bingbing, Cao, Yun, Cheng, Guoqiang, Wang, Laishuan, Hu, Liyuan, Mei, Hongfang, Lu, Yulan, Gong, Mengchun, Dong, Xinran, Zhou, Wenhao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920417/ https://www.ncbi.nlm.nih.gov/pubmed/35026772 http://dx.doi.org/10.1097/CM9.0000000000001959 |
Ejemplares similares
-
Association Between Expanded Genomic Sequencing Combined With Hearing Screening and Detection of Hearing Loss Among Newborns in a Neonatal Intensive Care Unit
por: Zhu, Yunqian, et al.
Publicado: (2022) -
Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes?
por: Ma, Haiyan, et al.
Publicado: (2021) -
Overdosage of HNF1B Gene Associated With Annular Pancreas Detected in Neonate Patients With 17q12 Duplication
por: Xiao, Feifan, et al.
Publicado: (2021) -
Genetic identification of pathogenic variations of the DMD gene: a retrospective study from 10,481 neonatal patients based on next-generation sequencing data
por: Xiao, Tiantian, et al.
Publicado: (2021) -
Rare-variant collapsing analyses identified risk genes for neonatal acute respiratory distress syndrome
por: Chen, Huiyao, et al.
Publicado: (2022)