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Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation.
Not available
S-EPMC9053646
|
biostudies-literature
Cite
A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.
Not available
S-EPMC1087158
|
biostudies-literature
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Loss of RNA expression and allele-specific expression associated with congenital heart disease.
Not available
S-EPMC5052634
|
biostudies-literature
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Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes.
Not available
S-EPMC11142749
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biostudies-literature
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<i>GATA6</i> mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm.
Not available
S-EPMC7593088
|
biostudies-literature
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Outcomes from elective colorectal cancer surgery during the SARS-CoV-2 pandemic.
Not available
S-EPMC7753519
|
biostudies-literature
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De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Not available
S-EPMC4890146
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biostudies-literature
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Not available
S-EPMC5675000
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biostudies-literature
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Preoperative nasopharyngeal swab testing and postoperative pulmonary complications in patients undergoing elective surgery during the SARS-CoV-2 pandemic.
Not available
S-EPMC7717156
|
biostudies-literature
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Elective Cancer Surgery in COVID-19-Free Surgical Pathways During the SARS-CoV-2 Pandemic: An International, Multicenter, Comparative Cohort Study.
Not available
S-EPMC8189635
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biostudies-literature
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