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쓰리빌리언의 연구 논문을 확인해보세요.

Paper Title
Role of Genetic Testing in Diagnosis and Prognosis Prediction in Hypertrophic Cardiomyopathy in Korea
Journal Name, Publication year
Journal of Korean Medical Science, 2024
링크
https://jkms.org/DOIx.php?id=10.3346/jkms.2024.39.e313
Paper Title
The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
Journal Name, Publication year
Egyptian Journal of Medical Human Genetics, 2024
링크
https://jmhg.springeropen.com/articles/10.1186/s43042-024-00579-2
Paper Title
ADGRG1-related polymicrogyria syndrome: report on a large consanguineous family with a novel variant and review
Journal Name, Publication year
Egyptian Journal of Medical Human Genetics, 2024
링크
https://jmhg.springeropen.com/articles/10.1186/s43042-024-00499-1
Paper Title
A homozygous nonsense variant in the alternatively spliced VLDLR exon 4 causes a neurodevelopmental disorder without features of VLDLR cerebellar hypoplasia
Journal Name, Publication year
Journal of Human Genetics , 2024
링크
https://www.nature.com/articles/s10038-024-01279-w
Paper Title
High prevalence of ALPK3 premature terminating variants in Korean hypertrophic cardiomyopathy patients
Journal Name, Publication year
Front. Cardiovasc. Med., 2024
링크
https://www.frontiersin.org/journals/cardiovascular-medicine/articles/10.3389/fcvm.2024.1424551/full
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