GENETIC INSIGHTS INTO 3-M SYNDROME: A NEONATAL CASE REPORT
收藏NIAID Data Ecosystem2026-05-02 收录
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https://zenodo.org/records/14257937
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资源简介:
3-M syndrome is an uncommon autosomal recessive disorder. We present a case of a one-day-old infant with low birth weight, an enlarged head, and shortened limbs, initially suspected of skeletal dysplasia. Genetic testing confirmed the diagnosis of 3-M syndrome.
创建时间:
2024-12-02



