Results 141 to 150 of about 24,363 (274)

Preimplantation genetic testing for aneuploidy (PGT-A) and technology platform: does platform influence euploid call rates and/or subsequent pregnancy outcomes? [PDF]

, 2019
Eleni A. Greenwood, Charles E. McCulloch, Kaitlyn Wald, Salustiano Ribeiro, Phil Marsh, Marcelle I. Cedars, Mitchell P. Rosen   +6 more
openalex   +1 more source

Replacing Myths with Facts: Sex-Selective Abortion Laws in the United States [PDF]

, 2014
Sex selection is the practice of attempting to control the sex of one's offspring in order to achieve a desired sex. One method of sex selection is sex-selective abortion. Laws banning sex-selective abortion are proliferating in the United States.
Brian Citro, Jeff Gilson, Kelsey Stricker, Sital Kalantry   +3 more
core  

Incidence, Clinical Risk Factors, and Pregnancy Outcomes of Trophectoderm‐ and Inner Cell Mass–Poor‐Quality Blastocysts in Single Blastocyst Transfer Cycles: A Retrospective Cohort Study

Reproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
ABSTRACT Purpose To study incidence, clinical risk factors, and pregnancy outcomes of trophectoderm‐ and inner cell mass–poor‐quality blastocysts in single blastocyst transfer cycles. Design A retrospective cohort study included patients who underwent their first single blastocyst transfer cycle.
Longbin Chen, Yangqin Peng, Shuoping Zhang, Yifan Gu, Fei Gong, Ge Lin, Lizhi Leng   +6 more
wiley   +1 more source

Genetic investigations of autosomal recessive inherited ichthyosis impressed by fetal ultrasound: Exome sequencing and haplotype linkage analysis

Taiwanese Journal of Obstetrics & Gynecology
Objective: Ichthyosis are complex skin diseases, characterized by hyperkeratosis with various degrees of thickening, desquamation, and erythema. The prenatal diagnosis of ichthyosis is challenged due to the clinical and genetic heterogeneity and the late-
Ting-Yu Chang, Zhu Wei Lim, Yi-Tzu Chu, Wan-Ju Wu, Mei-Hui Lee, Shun-Ping Chang, Dong-Jay Lee, Wen-Hsiang Lin, Ming Ho, Jin-Chung Shih, Gwo-Chin Ma, Ming Chen   +11 more
doaj   +1 more source

Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing [PDF]

, 2022
Wanwisa van Dijk, Kasper Derks, Marion Drüsedau, Jeroen Meekels, Rebekka M. Koeck, Rick Essers, J. Dreesen, Edith Coonen, Christine de Die‐Smulders, Servi J.C. Stevens, Han G. Brunner, Arthur van den Wijngaard, Aimée Paulussen, Masoud Zamani Esteki   +13 more
openalex   +1 more source

Assisted Reproductive Technology in Japan: A Summary Report for 2023 by the Committee on Professional Scientific Conduct and Clinical Ethics of the Japan Society of Obstetrics and Gynecology

Reproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
In 2023, the second year of insurance coverage, the registry recorded the highest numbers of treatment cycles and newborns. Effective registry systems planned for 2026 will enable comprehensive evaluation of emerging trends in Japanese ART practice. ABSTRACT Purpose To summarize assisted reproductive technology (ART) data for 2023 collected through the
Yukiko Katagiri, Seung Chik Jwa, Akira Kuwahara, Takeshi Iwasa, Masanori Ono, Keiichi Kato, Hiroshi Kishi, Yoshimitsu Kuwabara, Fuminori Taniguchi, Miyuki Harada, Akira Iwase, Norihiro Sugino   +11 more
wiley   +1 more source

O-287 Preimplantation genetic testing for monogenic disease (PGT-M) where results are only based upon analysis of linked polymorphisms/haplotypes risks serious diagnostic errors [PDF]

, 2023
Ayman Haj Ali, M Ampiah, H Abdous, D Babariya, A Raberi, Dagan Wells   +5 more
openalex   +1 more source

Primary Coenzyme Q10 Deficiency [PDF]

, 2017
open4siCLINICAL CHARACTERISTICS: Primary coenzyme Q10 (CoQ10) deficiency is usually associated with multisystem involvement, including neurologic manifestations such as fatal neonatal encephalopathy with hypotonia; a late-onset slowly progressive ...
Doimo, Mara, Navas, P., Salviati, Leonardo, Trevisson, Eva   +3 more
core  

A Case of Cystic Fibrosis in a Japanese Man With Congenital Bilateral Absence of the Vas Deferens and Recurrent Pancreatitis Caused by a Homozygous c.1210‐11 T > G Variant of the Cystic Fibrosis Transmembrane Conductance Regulator Gene

Reproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
ABSTRACT Case We herein report a rare case of a Japanese man diagnosed with cystic fibrosis (CF) following a workup for male infertility and recurrent pancreatitis and discuss the clinical and diagnostic implications in a population wherein CF is exceptionally rare. A 27‐year‐old Japanese man who presented with azoospermia underwent clinical evaluation,
Tomoki Saito, Shinnosuke Kuroda, Teppei Takeshima, Takashi Kawahara, Junichi Teranishi, Jurii Karibe, Fuka Anzai, Miki Tanoshima, Kazuhide Makiyama, Yasushi Yumura   +9 more
wiley   +1 more source

Successful Live Birth Following PGT‐SR in a Couple Who Were Both Carriers of Balanced Reciprocal Translocations Identified During Recurrent Pregnancy Loss Workup: A Case Report

Reproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
ABSTRACT Case A non‐consanguineous couple with recurrent pregnancy loss was found to be carriers of two different balanced reciprocal translocations: 46,XX,t(13;16)(q14;q23) and 46,XY,t(4;12)(q21.1;q15). They underwent IVF with PGT‐SR, from which seven blastocysts were obtained.
Hiroaki Negishi, Daisuke Higeta, Satoh Maki, Setsuko Satoh, Youko Matsumiya, Nanami Takano, Hidemi Yokota, Mikako Yokota, Yoshimasa Yokota   +8 more
wiley   +1 more source