Results 241 to 250 of about 142,560 (388)

The PreGen Research Program: Implementing Prenatal Genomic Testing in Australia—A Commentary

open access: yesAustralian and New Zealand Journal of Obstetrics and Gynaecology, EarlyView.
ABSTRACT Prenatal genomic sequencing, which can provide a significantly increased diagnostic rate for fetal structural anomaly (FSA) compared with karyotype and microarray, is not available uniformly across Australia. PreGen, a 5‐year translational research program, has identified significant barriers to implementation including access to funding, the ...
Sarah Long   +17 more
wiley   +1 more source

The evolution of prenatal Whole Exome Sequencing: from cytogenetics to precision medicine. [PDF]

open access: yesArch Clin Cases
Săbău ID   +6 more
europepmc   +1 more source

Methylation‐specific digital karyotyping of HPV16E6E7‐expressing human keratinocytes identifies novel methylation events in cervical carcinogenesis

open access: yesJournal of Pathology, 2013
R. Steenbergen   +10 more
semanticscholar   +1 more source

The Effect of Assisted Reproductive Technologies on Human Sex Ratios

open access: yesAustralian and New Zealand Journal of Obstetrics and Gynaecology, EarlyView.
ABSTRACT Background Modern assisted reproductive technology (ART), including pre‐implantation genetic testing for aneuploidy (PGT‐A), has opened new avenues in understanding early embryonic events and has simultaneously raised questions about the impact of ART itself on sex ratios.
Ektoras X. Georgiou   +6 more
wiley   +1 more source

Plain Language Summary of the ACCEPT Guideline for the Management of Recurrent Pregnancy Loss

open access: yesAustralian and New Zealand Journal of Obstetrics and Gynaecology, EarlyView.
ABSTRACT Recurrent pregnancy loss (RPL) is when a woman experiences two or more pregnancy losses. Investigating for causes of RPL can provide an explanation and possible treatment options. This is a summary of Parts 1 and 2 of Australasian Recurrent Pregnancy Loss Clinical Management Guidelines in an easy‐to‐read patient friendly format. These original
Adriana Suker   +4 more
wiley   +1 more source

Application of Optical Genome Mapping for the Diagnosis and Risk Stratification of Myeloid and Lymphoid Malignancies. [PDF]

open access: yesInt J Mol Sci
Ballesta-Alcaraz L   +7 more
europepmc   +1 more source

Clonal heterogeneity as detected by metaphase karyotyping is an indicator of poor prognosis in acute myeloid leukemia.

open access: yesJournal of Clinical Oncology, 2013
T. Bochtler   +13 more
semanticscholar   +1 more source

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