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40 积分 2026-06-11 加入
The ontogenesis of language lateralization and its relation to handedness
23天前
已完结
Novel HYLS1 variants associated with Joubert syndrome suggest potential genotype-phenotype correlates
1个月前
已完结
Test the grandfather! Incidental in-frame DMD deletions in three asymptomatic families
1个月前
已关闭
Analysing tumours for genetic diagnosis in mosaic neurofibromatosis type 1
1个月前
已完结
Clinical and genetic spectrum of RNF216-related disorder: a new case and literature review
1个月前
已完结
Novel HYLS1 variants associated with Joubert syndrome suggest potential genotype-phenotype correlates
1个月前
已完结
Diagnosis and treatment of Diamond-Blackfan anemia and Pierre-Robin sequence caused by a novel mutation of RPS28 gene
3个月前
已完结
Diagnosis and treatment of Diamond-Blackfan anemia and Pierre-Robin sequence caused by a novel mutation of RPS28 gene
3个月前
已关闭
The Molecular and Genetic Basis of Fibroblast Growth Factor Receptor 3 Disorders: The Achondroplasia Family of Skeletal Dysplasias, Muenke Craniosynostosis, and Crouzon Syndrome with Acanthosis Nigricans
4个月前
已关闭
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