Lv11
50 积分 2024-10-08 加入
[Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT]
2小时前
求助中
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations
27天前
已完结
Triploid pregnancy–Clinical implications
28天前
已完结
Trisomy 13
1个月前
已关闭
Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: A genotype-phenotype analysis
1个月前
已完结
2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay
1个月前
已完结
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations
1个月前
已完结
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