A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility

Y Sun, Y Zeng, H Chen, Z Zhou, J Fu, Q Sang… - Journal of Assisted …, 2021 - Springer
Purpose We aimed to identify pathogenic variants in two infertile sisters in a family with a
thin zona pellucida (ZP) phenotype. Methods Whole-exome sequencing was performed in …
被引用次数：12 相关文章

A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility

Y Sun, Y Zeng, H Chen, Z Zhou, J Fu… - Journal of Assisted …, 2021 - search.proquest.com
Purpose We aimed to identify pathogenic variants in two infertile sisters in a family with a
thin zona pellucida (ZP) phenotype. Methods Whole-exome sequencing was performed in …

A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility

Y Sun, Y Zeng, H Chen, Z Zhou, J Fu… - Journal of assisted …, 2021 - pubmed.ncbi.nlm.nih.gov
Purpose We aimed to identify pathogenic variants in two infertile sisters in a family with a
thin zona pellucida (ZP) phenotype. Methods Whole-exome sequencing was performed in …

A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility.

Y Sun, Y Zeng, H Chen, Z Zhou, J Fu… - Journal of Assisted …, 2021 - europepmc.org
Purpose We aimed to identify pathogenic variants in two infertile sisters in a family with a
thin zona pellucida (ZP) phenotype. Methods Whole-exome sequencing was performed in …

A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility.

Y Sun, Y Zeng, H Chen, Z Zhou, J Fu… - Journal of Assisted …, 2021 - search.ebscohost.com
Purpose: We aimed to identify pathogenic variants in two infertile sisters in a family with a
thin zona pellucida (ZP) phenotype. Methods: Whole-exome sequencing was performed in …
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[HTML][HTML] A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility

Y Sun, Y Zeng, H Chen, Z Zhou, J Fu… - Journal of Assisted …, 2021 - ncbi.nlm.nih.gov
Purpose We aimed to identify pathogenic variants in two infertile sisters in a family with a
thin zona pellucida (ZP) phenotype. Methods Whole-exome sequencing was performed in …