官方服务：
资源简介：
to analyze the genetic constitution of embryos of a balanced translocation family
应用场景：
创建时间：
2021-03-04
相关数据集
New protocol based on massive parallel sequencing for aneuploidy screening of preimplantation human embryos
Novel next-generation sequencing procedures have rapidly emerged into the preimplantation genetic screening framework. This work presents the design and validation of a new low-coverage whole-genome s
DataCite Commons2020-09-02 更新80
SPTB family
Integrative Preimplantation Genetic Testing Analysis for a Chinese Family with Hereditary Spherocytosis Caused by a Novel Splicing Variant of SPTB
NIAID Data Ecosystem50
Preimplantation genetic diagnosis for cystic fibrosis: a case report
Cystic fibrosis is an autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator gene. This disorder produces a variable phenotype including lung disea
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The Influence of Single Nucleotide Polymorphism Microarray-Based Molecular Karyotype on Preimplantation Embryonic Development Potential
In order to investigate the influence of the molecular karyotype based on single nucleotide polymorphism (SNP) microarray on embryonic development potential in preimplantation genetic diagnosis (PGD),
Figshare2016-01-15 更新50
Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier. Homo sapiens
Objective: To prove the ability to distinguish between balanced and normal chromosomes in embryos from a translocation carrier. Design: Case report. Setting: Academic center for reproductive medicine.
NIAID Data Ecosystem40
