Associated Papers
Genetic Polymorphisms of LPCAT1, CHPT1 and PCYT1B and Risk of Neonatal Respiratory Distress Syndrome among a Chinese Han Population.
Shen W et al.
Pediatrics and Neonatology, 2020
Frequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newborn.
Wang M et al.
Respiratory Research, 2020
32054482 (PubMed )
Supplement: 12931_2020_1314_MOESM1_ESM.xlsx › S6
Study on the Relationship Between Respiratory Distress Syndrome and SP-A1 (rs1059057) Gene Polymorphism in Mongolian Very Premature Infants.
Wang X et al.
Frontiers in Pediatrics, 2020
Genetic Polymorphisms of SP-A, SP-B, and SP-D and Risk of Respiratory Distress Syndrome in Preterm Neonates.
Chang HY et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2016
Long-range PCR based sequencing of the highly homologous genes, SFTPA1 and SFTPA2.
Horton CJ et al.
Molecular and Cellular Probes, 0
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