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UnknownBirth data accessibility via primary care health records to classify health status in a multi-ethnic population of children: an observational study.
Not available
S-EPMC4353844 | biostudies-literature
UnknownDe novo variants in <i>KDM2A</i> cause a syndromic neurodevelopmental disorder.
Not available
S-EPMC11998838 | biostudies-literature
UnknownDe novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Not available
S-EPMC12824617 | biostudies-literature
UnknownDuration of androgen deprivation therapy with postoperative radiotherapy for prostate cancer: a comparison of long-course versus short-course androgen deprivation therapy in the RADICALS-HD randomised trial.
Not available
S-EPMC7616389 | biostudies-literature
UnknownBiallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Not available
S-EPMC10932913 | biostudies-literature
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