Lv1
46 积分 2023-05-23 加入
Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency Detected by Long-Read Sequencing and Phenotypes Correlation
18小时前
已完结
Comprehensive Assays for Incontinentia Pigmenti Using Long-Read Sequencing and Its Application in Preimplantation Genetic Testing
1天前
已完结
COX15 deficiency causes oocyte ferroptosis
10个月前
已完结
Function of seminal vesicles and their role on male fertility
11个月前
已关闭
Genetic evaluation of the azoospermic or severely oligozoospermic male
11个月前
已完结
Re: Increased Frequency of CFTR Gene Mutations Identified in Indian Infertile Men with Non-CBAVD Obstructive Azoospermia and Spermatogenic Failure
11个月前
已完结
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
11个月前
已完结
Chromosome 16 Abnormalities in Embryos and in Sperm from a Male with a Fragile Site at 16q22.1
1年前
已完结
Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
1年前
已完结
Premature ovarian insufficiency
1年前
已完结
Optimization of Fuel Cell Performance Using Computational Fluid Dynamics
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