Lv1
28 积分 2025-07-24 加入
A novel de novo heterozygous deletion at 13q14.2-q21.1 in two siblings with mild intellectual disability
1天前
已完结
Detecting Androgenetic Origin of the Genome via Single-Nucleotide Polymorphism-Based Cell-Free DNA Screening in Dichorionic Diamniotic Twin Pregnancies With Complete Hydatidiform Moles and a Coexisting Normal Fetus: A Three-Case Report
16天前
已完结
The Key Roles of Makorin RING Finger Protein 3 (MKRN3) Duringthe Development of Pubertal Initiation and Central PrecociousPuberty (CPP)
3个月前
已完结
Molecular genetics of congenital heart disease
3个月前
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
7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
7个月前
已完结
A NEW OBSERVATION OF 13q DELETION SYNDROME: SEVERE UNDESCRIBED FEATURES
1年前
已关闭
First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic review
1年前
已关闭
[Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease]
1年前
已完结
Cognitive and Behavioral Phenotype of a Young Man With a Chromosome 13 Deletion del(13)(q21.32q31.1)
1年前
已关闭
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