[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis]

Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2024

Diagnostic yield using whole-genome sequencing and in-silico panel of 281 genes associated with non-immune hydrops fetalis in clinical setting.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2022

Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.

Journal of internal medicine·2020

Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.

Human reproduction (Oxford, England)·2014

No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation·2014

An expression signature at diagnosis to estimate prostate cancer patients' overall survival.

Prostate cancer and prostatic diseases·2014

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

Lakartidningen·2026

[Rare manifestations of giant cell arteritis].

Lakartidningen·2026

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

Lakartidningen·2026

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

Lakartidningen·2026

[Postoperative atrial fibrillation after open heart surgery].

Lakartidningen·2026

[Interaction between psychotic patients and AI-driven chatbots].

Lakartidningen·2026

SMURF1 alleviates preeclampsia by suppressing ferroptosis in trophoblast cells via mediating ubiquitination of FLT1.

Cellular signalling·2026

Risk of monozygotic twinning associated with different blastocyst transfer strategies in single embryo transfer cycles.

European journal of obstetrics, gynecology, and reproductive biology·2026

Singleton freemartinism in cattle: A structured narrative review and historical case reappraisal.

Theriogenology·2026

The Building and Application of a Machine Learning Model on Predicting Euploid Blastocysts in IVF Treatments Without PGT-A.

Reproductive sciences (Thousand Oaks, Calif.)·2026

A context-specific evaluation of polygenic embryo screening in best-prognosis preimplantation genetic testing cycles.

Human reproduction open·2026

Familial 46,XY disorder of sex development due to a novel CYB5A variant: a rare cause of isolated 17,20-lyase deficiency.

JCEM case reports·2026

Related Experiment Videos

[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis]

Related Concept Videos

Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting.

Diagnostic yield using whole-genome sequencing and in-silico panel of 281 genes associated with non-immune hydrops fetalis in clinical setting.

Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.

Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.

No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency.

An expression signature at diagnosis to estimate prostate cancer patients' overall survival.

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

[Rare manifestations of giant cell arteritis].

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

[Postoperative atrial fibrillation after open heart surgery].

[Interaction between psychotic patients and AI-driven chatbots].

SMURF1 alleviates preeclampsia by suppressing ferroptosis in trophoblast cells via mediating ubiquitination of FLT1.

Risk of monozygotic twinning associated with different blastocyst transfer strategies in single embryo transfer cycles.

Singleton freemartinism in cattle: A structured narrative review and historical case reappraisal.

The Building and Application of a Machine Learning Model on Predicting Euploid Blastocysts in IVF Treatments Without PGT-A.

A context-specific evaluation of polygenic embryo screening in best-prognosis preimplantation genetic testing cycles.

Familial 46,XY disorder of sex development due to a novel CYB5A variant: a rare cause of isolated 17,20-lyase deficiency.

Related Experiment Videos

[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis]

Related Concept Videos

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