Lv4
800 积分 2022-09-20 加入
Nephronophthisis: a pathological and genetic perspective
5天前
已完结
Nephronophthisis: a pathological and genetic perspective
7天前
已完结
Identification of a Splicing Variant c.3813-3A>G in NPHP3 by Reanalysis of Whole Exome Sequencing in a Chinese Boy with Nephronophthisis
7天前
已完结
Neurosurgical intervention for the Meckel-Gruber Syndrome: A systematic review
9天前
已完结
Craniosynostosis in molecularly diagnosed Kabuki syndrome: Prevalence and clinical implications
17天前
已完结
OCA2基因复合杂合变异致眼皮肤白化病1例患儿的遗传学分析
17天前
已完结
PCDH12基因复合杂合变异致间脑-中脑连接处发育不良综合征1型2例患儿的临床特征与遗传学分析
17天前
已完结
遗传性痉挛性截瘫84型1例患者的 PI4KA基因变异分析
17天前
已完结
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics
18天前
已完结
Genetics of ovarian insufficiency and defects of folliculogenesis
18天前
已完结
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