火宝
Lv42
460 积分
2022-05-03 加入
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SPTLC1 Mutations Associated with Early Onset Amyotrophic Lateral Sclerosis
1天前
已关闭
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Mechanisms of congenital hearing loss caused by GJB2 gene mutations and current progress in gene therapy
2个月前
已完结
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A rare viable delivery of a 45,X/46,XY mosaicism female with complete gonadal dysgenesis after receiving oocyte donation and overcoming multiple pregnancy complications
2个月前
已完结
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Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly
2个月前
已关闭
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Whole-exome sequencing identifies genetic variants of hearing loss in 113 Chinese families
3个月前
已完结
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Towards improved genetic diagnosis of human differences of sex development
4个月前
已完结
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[Live birth achieved by oocyte donation in a patient with 45,X/46,XY mixed gonadal dysgenesis: A case report and literature review]
6个月前
已关闭
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48 XXYY KARYOTYPE IN A FEMALE WITH RECURRENT PREGNANCY LOSS: A CASE REPORT
9个月前
已关闭
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De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias
1年前
已关闭
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De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias
1年前
已完结