Results 101 to 110 of about 5,754 (180)

Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 Gene. [PDF]

Cell J, 2021
Tabatabaei Z, Karbalaie KH, Habibzadeh P, Farazi Fard MA, Faghihi MA, Nasr Esfahani MH.   +5 more
europepmc   +1 more source

Combined SNP parental haplotyping and intensity analysis identifies meiotic and mitotic aneuploidies and frequent segmental aneuploidies in preimplantation human embryos

Scientific Reports
Genome-wide single nucleotide polymorphism (SNP) genotyping using microarrays and karyomapping (parental haplotyping) is a universal linkage-based method for preimplantation genetic testing of monogenic disease (PGT-M) and identification of chromosome ...
Alan H. Handyside, Louise Newnham, Matthew Newnham, Dominika Henning, Jan Velebny, Jan Pozdena, Jindriska Krmelova, Jakub Horak   +7 more
doaj   +1 more source

Evaluating the application value of NGS-based PGT-A by screening cryopreserved MDA products of embryos from PGT-M cycles with known transfer outcomes. [PDF]

J Assist Reprod Genet, 2022
Shen X, Chen D, Ding C, Xu Y, Fu Y, Cai B, Wang Y, Wang J, Li R, Guo J, Pan J, Zhang H, Zeng Y, Zhou C.   +13 more
europepmc   +1 more source

Development and clinical application of a preimplantation genetic testing for monogenic disease (PGT-M) for beta thalassemia in Vietnam. [PDF]

J Assist Reprod Genet, 2021
Mai AD, Harton GL, Harton GL, Quang VN, Van HN, Thi NH, Thuy NP, Le Thi TH, Minh DN, Quoc QT.   +9 more
europepmc   +1 more source

A comprehensive PGT-M strategy for ADPKD patients with de novo PKD1 mutations using affected embryo or gametes as proband. [PDF]

J Assist Reprod Genet, 2021
Wang Y, Zhai F, Guan S, Yan Z, Zhu X, Kuo Y, Wang N, Zhi X, Lian Y, Huang J, Jia J, Liu P, Li R, Qiao J, Yan L.   +14 more
europepmc   +1 more source

The complexity of conditions for which patients pursue PGT-M: a modern snapshot [PDF]

Fertility and Sterility, 2019
Lauren Spor, Kristina Cotter, Stephanie Bivona, Ana Cervero, Jose Antonio Martinez-Conejero, Cengiz Cinnioglu, Alyssa Snider   +6 more
openaire   +1 more source

A novel homozygous splicing variant in FREM1 expands the phenotypic spectrum of BNAR syndrome: functional validation and successful PGT-M. [PDF]

BMC Med Genomics
Yan L, Liu Y, Zhang Y, Han C, Cao J, Zou J, Luo H, Li H.   +7 more
europepmc   +1 more source

Effect of endometrial thickness changes on clinical pregnancy rates after progesterone administration in a single frozen-thawed euploid blastocyst transfer cycle using natural cycles with luteal support for PGT-SR- and PGT-M-assisted reproduction: a retrospective cohort study. [PDF]

Reprod Biol Endocrinol, 2021
Jin Z, Li J, Yang E, Shi H, Bu Z, Niu W, Wang F, Huo M, Song H, Zhang Y.   +9 more
europepmc   +1 more source

Timing day-3 vitrification for PGT-M embryos: pre- or post-blastomere biopsy? [PDF]

J Assist Reprod Genet, 2020
Aizer A, Shimon C, Dratviman-Storobinsky O, Shani H, Harel Inbar N, Maman E, Orvieto R.   +6 more
europepmc   +1 more source

Combined Preimplantation Genetic Testing for Aneuploidy (PGT-A) and Monogenic Disorders (PGT-M) to Prevent Autosomal Dominant Polycystic Kidney Disease After Kidney Transplant. [PDF]

Cureus
Elbanna W, Azmy O, Elhinnawi MA.
europepmc   +1 more source