Lv1
60 积分 2021-10-14 加入
一个双侧耳甲腔型小耳畸形家系遗传学及临床表型分析
13天前
已完结
Classification of Brain Magnetic Resonance Imaging Abnormalities and Spectrum of Neurological Findings in a Cohort with Copy Number Variation-Related Disorders
1个月前
已关闭
羊水产前诊断46，XY，rec(18)dup(18q)inv(18)(p11q12)一例
1个月前
已完结
The molecular mechanisms of recombinant chromosome 18 with parental pericentric inversions and a review of the literature
1个月前
已完结
Enhancing clinical decision-making for CNVs of uncertain significance in neurodevelopmental disorders: the relevance (or uselessness) of scoring and segregating
1个月前
已完结
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots
1个月前
已完结
[Prenatal diagnosis and genetic analysis of a fetus with der(X)t(X;Y)(p22.3;q11.2)]
1个月前
已完结
Czech family confirms the new 1p36.13‐1p36.12 microdeletion syndrome
1个月前
已完结
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay
1个月前
已完结
De novo triplication at 1p36.23p36.22 further refines the dosage sensitive region of overlap in Setleis syndrome (focal facial dermal dysplasia type III)
1个月前
已完结
Metal-Free Synthesis of Unsymmetrical Ureas and Carbamates from CO2 and Amines via Isocyanate Intermediates
7个月前
已采纳
Clinical and genetic features of retinoschisis in 120 families withRS1mutations
7个月前
已驳回
An integrated approach for line balancing and AGV scheduling towards smart assembly systems
7个月前
已采纳
六方氮化硼纳米颗粒增强生物聚合物纳米复合材料的结构，形态和介电性能
7个月前
已采纳
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