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10 积分 2025-07-24 加入
The Key Roles of Makorin RING Finger Protein 3 (MKRN3) Duringthe Development of Pubertal Initiation and Central PrecociousPuberty (CPP)
4小时前
待确认
Molecular genetics of congenital heart disease
6小时前
已完结
Anomalous Origin of the Right Coronary Artery From Pulmonary Trunk in a Hypoplastic Left Heart Syndrome With 15q11.2 BP1-BP2 Microdeletion: A Novel Association
3个月前
已完结
Deciphering the RNA-binding protein interaction with the mRNAs encoded from human chromosome 15q11.2 BP1-BP2 microdeletion region
3个月前
已完结
A NEW OBSERVATION OF 13q DELETION SYNDROME: SEVERE UNDESCRIBED FEATURES
9个月前
已关闭
First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic review
9个月前
已关闭
[Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease]
9个月前
已完结
Cognitive and Behavioral Phenotype of a Young Man With a Chromosome 13 Deletion del(13)(q21.32q31.1)
9个月前
已关闭
Hand Involvement in 13q Deletion Syndrome
9个月前
已关闭
13q deletion syndrome in an adult mentally retarded patient
9个月前
已关闭
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