Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: A case report

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Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: A case report

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Cyanosis is usually associated with serious conditions requiring urgent treatment in the neonatal intensive care unit (NICU). Hemoglobin M (Hb M) disease is one type of congenital methemoglobinemia characterized by cyanosis. | Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: A case report

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Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: A case report

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Đang chuẩn bị liên kết để tải về tài liệu: Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: A case report

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

Detection of internal exon deletion with exon Del

Comparing variant calling algorithms for target-exon sequencing in a large sample

Events of alternative splicing in head and neck cancer via RNA sequencing – an update

Routine performance and errors of 454 HLA exon sequencing in diagnostics

Genetic mutational analysis of pediatric acute lymphoblastic leukemia from a single center in China using exon sequencing

Gene promoter and exon DNA methylation changes in colon cancer development – mRNA expression and tumor mutation alterations

Improving RNA-Seq expression estimation by modeling isoform- and exon-specific read sequencing rate

Novel genomic resources for shelled pteropods: A draft genome and target capture probes for Limacina bulimoides, tested for cross-species relevance

Patients harboring uncommon EGFR exon 19 deletion-insertion mutations respond well to first-generation EGFR inhibitors and osimeritinib upon acquisition of T790M

Đang chuẩn bị liên kết để tải về tài liệu:
Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: A case report