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Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers
Author(s) -
YueQiu Tan,
Ke Tan,
S.- P. Zhang,
Fei Gong,
Dehua Cheng,
Bo Xiong,
CanZhong Lu,
Xiaoning Tang,
K Luo,
Ge Lin,
G. X. Lu
Publication year - 2013
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/det271
Subject(s) - preimplantation genetic diagnosis , chromosomal translocation , single nucleotide polymorphism , biology , blastomere , snp array , snp , embryo , embryo transfer , fluorescence in situ hybridization , genetics , microarray , biopsy , andrology , gene , genotype , medicine , pathology , embryogenesis , gene expression , chromosome
Is preimplantation genetic diagnosis (PGD) for translocation carriers more effective when done with a single-nucleotide polymorphism (SNP) array using trophectoderm (TE) biopsy and frozen embryo transfer (FET) compared with traditional PGD based on fluorescence in situ hybridization (FISH-PGD) using blastomere biopsy and fresh embryo transfer?

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