[Genetic, biochemical and genomic prenatal diagnosis in genetic defects]

Cancer treatments-related factors for subsequent soft-tissue sarcoma in childhood cancer survivors.

ESMO open·2026

TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study.

NPJ precision oncology·2021

Olfactory dysfunction in SARS-CoV-2 infection: Focus on odorant specificity and chronic persistence.

American journal of otolaryngology·2021

Treatment-related fertility impairment in long-term female childhood, adolescent and young adult cancer survivors: investigating dose-effect relationships in a European case-control study (PanCareLIFE).

Human reproduction (Oxford, England)·2021

A surface plasmon field-enhanced fluorescence reversible split aptamer biosensor.

The Analyst·2017

Influence of myelin proteins on the structure and dynamics of a model membrane with emphasis on the low temperature regime.

The Journal of chemical physics·2014

[Gynecologic urology].

Gynakologische Rundschau·1991

[Does fetal reaction to vibro-acoustic stimulation depend on its activity state?].

Gynakologische Rundschau·1991

[Vulvar cancer. Bern university gynecologic clinic patients treated 1978 to 1987].

Gynakologische Rundschau·1991

[Acceptance and subjective well-being with a norgestimate combination pill].

Gynakologische Rundschau·1991

[Local administration of low-dose estriol and vital Lactobacillus acidophilus in postmenopause].

Gynakologische Rundschau·1991

[Is there a correlation in the frequent association of neuroblastoma-fetal malformations?].

Gynakologische Rundschau·1991

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Biology of sex differences·2026

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Ophthalmology science·2026

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Journal of assisted reproduction and genetics·2026

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

American journal of human genetics·2026

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Cancer treatments-related factors for subsequent soft-tissue sarcoma in childhood cancer survivors.

TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study.

Olfactory dysfunction in SARS-CoV-2 infection: Focus on odorant specificity and chronic persistence.

Treatment-related fertility impairment in long-term female childhood, adolescent and young adult cancer survivors: investigating dose-effect relationships in a European case-control study (PanCareLIFE).

A surface plasmon field-enhanced fluorescence reversible split aptamer biosensor.

Influence of myelin proteins on the structure and dynamics of a model membrane with emphasis on the low temperature regime.

[Gynecologic urology].

[Does fetal reaction to vibro-acoustic stimulation depend on its activity state?].

[Vulvar cancer. Bern university gynecologic clinic patients treated 1978 to 1987].

[Acceptance and subjective well-being with a norgestimate combination pill].

[Local administration of low-dose estriol and vital Lactobacillus acidophilus in postmenopause].

[Is there a correlation in the frequent association of neuroblastoma-fetal malformations?].

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

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