Genetic counselling: the blueprint for a more certain future

Is routine cocaine testing justified in patients with septal perforation?

Rhinology·2025

Person-centred care in the management of imaging-related anxiety in diagnostic radiography: A scoping review exploring cancer and non-cancer populations.

Radiography (London, England : 1995)·2025

Adverse Effects of Steroid Therapy in Sudden Sensorineural Hearing Loss: A Scoping Review.

Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery·2025

Is nasal closure an effective treatment for severe refractory epistaxis in HHT? A scoping review and narrative synthesis.

Rhinology·2025

Circulating soluble fibroblast activation protein (FAP) levels are independent of cardiac and extra-cardiac FAP expression determined by targeted molecular imaging in patients with myocardial FAP activation.

International journal of cardiology·2024

The role of large cavity sinus surgery in the management of chronic rhinosinusitis in non-steroidal anti-inflammatory drug exacerbated respiratory disease: a single-centre experience and long-term outcomes.

The Journal of laryngology and otology·2022

Hyperexcitability in hippocampal CA1 pyramidal cells OF Fmr1 knockout mice emerges during late postnatal development.

Neuroscience·2026

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Related Experiment Videos

Genetic counselling: the blueprint for a more certain future

Related Concept Videos

Is routine cocaine testing justified in patients with septal perforation?

Person-centred care in the management of imaging-related anxiety in diagnostic radiography: A scoping review exploring cancer and non-cancer populations.

Adverse Effects of Steroid Therapy in Sudden Sensorineural Hearing Loss: A Scoping Review.

Is nasal closure an effective treatment for severe refractory epistaxis in HHT? A scoping review and narrative synthesis.

Circulating soluble fibroblast activation protein (FAP) levels are independent of cardiac and extra-cardiac FAP expression determined by targeted molecular imaging in patients with myocardial FAP activation.

The role of large cavity sinus surgery in the management of chronic rhinosinusitis in non-steroidal anti-inflammatory drug exacerbated respiratory disease: a single-centre experience and long-term outcomes.

Hyperexcitability in hippocampal CA1 pyramidal cells OF Fmr1 knockout mice emerges during late postnatal development.

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Related Experiment Videos

Genetic counselling: the blueprint for a more certain future

Related Concept Videos

Related Articles