ORIGINAL RESEARCH
Published on 19 Apr 2022
Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort
doi 10.3389/fgene.2022.818241
- 7,084 views
- 16 citations
- Frontiers in Genetics
- Genetics of Common and Rare Diseases
- Research Topics
- Genetic and Environmental Factors in the Occurrence of Neonatal Disorders - Volume I
Genetic and Environmental Factors in the Occurrence of Neonatal Disorders - Volume I
10k
Total downloads
52k
Total views and downloads
Articles
ORIGINAL RESEARCH
Published on 24 Mar 2022
SNP–SNP Interactions of Surfactant Protein Genes in Persistent Respiratory Morbidity Susceptibility in Previously Healthy Children
doi 10.3389/fgene.2022.815727
- 1,321 views
- 6 citations
CASE REPORT
Published on 14 Mar 2022
Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1
doi 10.3389/fgene.2022.843931
- 1,926 views
- 3 citations
ORIGINAL RESEARCH
Published on 10 Mar 2022
Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogressive Cerebellar Ataxia Syndrome
doi 10.3389/fgene.2022.821587
- 2,730 views
- 6 citations
ORIGINAL RESEARCH
Published on 07 Mar 2022
LncRNA-RMST Functions as a Transcriptional Co-regulator of SOX2 to Regulate miR-1251 in the Progression of Hirschsprung's Disease
doi 10.3389/fped.2022.749107
- 1,796 views
- 12 citations
CASE REPORT
Published on 02 Feb 2022
Renal Involvement in IPEX Syndrome With a Novel Mutation of FOXP3: A Case Report
doi 10.3389/fgene.2021.752775
- 1,794 views
- 4 citations
ORIGINAL RESEARCH
Published on 18 Oct 2021
Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes?
doi 10.3389/fped.2021.727301
- 47,495 views
- 6 citations
ORIGINAL RESEARCH
Published on 04 Oct 2021
Single Nucleotide Polymorphisms Interactions of the Surfactant Protein Genes Associated With Respiratory Distress Syndrome Susceptibility in Preterm Infants
doi 10.3389/fped.2021.682160
- 2,113 views
- 9 citations
ORIGINAL RESEARCH
Published on 04 Aug 2021
High-Frequency Exon Deletion of DNA Cross-Link Repair 1C Accounting for Severe Combined Immunodeficiency May Be Missed by Whole-Exome Sequencing
doi 10.3389/fgene.2021.677748
- 2,040 views
- 5 citations
ORIGINAL RESEARCH
Published on 02 Jul 2021
Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information
doi 10.3389/fgene.2021.689071
- 3,326 views
- 32 citations
Published in
Frontiers in Genetics
Genetics of Common and Rare Diseases
Participating Journals
Frontiers in Pediatrics
- 2.1 impact factor
- 3.6 citescore