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Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Not available
S-EPMC10183469
|
biostudies-literature
Cite
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Not available
S-EPMC10806447
|
biostudies-literature
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Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.
Not available
S-EPMC5778085
|
biostudies-literature
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Global Retinoblastoma Presentation and Analysis by National Income Level.
Not available
S-EPMC7047856
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biostudies-literature
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Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder.
Not available
S-EPMC11451386
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biostudies-literature
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Use of Telemedicine for Postdischarge Assessment of the Surgical Wound: International Cohort Study, and Systematic Review With Meta-analysis.
Not available
S-EPMC10174106
|
biostudies-literature
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Global variation in anastomosis and end colostomy formation following left-sided colorectal resection.
Not available
S-EPMC6921967
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biostudies-literature
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Tocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC8084355
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biostudies-literature
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Azithromycin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC7884931
|
biostudies-literature
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Convalescent plasma in patients admitted to hospital with COVID-19 (RECOVERY): a randomised controlled, open-label, platform trial.
Not available
S-EPMC8121538
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biostudies-literature
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