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70 积分 2024-03-28 加入
Molecular and clinical characteristics of pediatric patients with primary congenital hypothyroidism: novel genetic variants and the genotype-phenotype association
5天前
已完结
Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism
5天前
已完结
ALG8-CDG: Advances in Molecular and Prenatal Phenotyping Facilitate Prenatal Diagnosis and Genetic Counseling
1个月前
已完结
Cesarean section and risks of overweight and obesity in school-aged children: a population-based study
1个月前
已完结
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencing
1个月前
已完结
A Novel Variant in Pulmonary Alveolar Microlithiasis With Disseminated Pseudomonas Infection
3个月前
已完结
Newborn Genetic Screening Revealed Increased Levels of Biochemical Indicators in Carriers of Heterozygous Variants
3个月前
已完结
Newborn Genetic Screening Revealed Increased Levels of Biochemical Indicators in Carriers of Heterozygous Variants
3个月前
已完结
Carriers of autosomal recessive conditions: are they really ‘unaffected?’
4个月前
已完结
Polygenic Risk Scores and Hearing Loss Phenotypes in Children
5个月前
已完结
A Janus dual-atom catalyst for electrocatalytic oxygen reduction and evolution
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