The genetic testing of children

The distribution of healthcare workforces relative to population ill health in England: Repeated cross-sectional analysis of Census data 2001-2021.

Public health·2025

Prevalence of transthyretin cardiac amyloidosis in undifferentiated heart failure with preserved ejection fraction.

ESC heart failure·2024

The inflexible mind: A critical factor in understanding and addressing COVID-19 vaccine hesitancy.

Journal of psychiatric research·2024

An outbreak of SARS-CoV-2 in a public-facing office in England.

Occupational medicine (Oxford, England)·2023

Delayed tension pneumocephalus and pneumorrhacis after routine cervical spine surgery treated successfully without burr holes.

Annals of the Royal College of Surgeons of England·2023

The relationship between parental adverse childhood experiences and the health, well-being and development outcomes of their children: a systematic review.

Public health·2023

Cancer Variant Interpretation Group UK (CanVIG-UK): updates on an exemplar national subspecialty multidisciplinary network.

Journal of medical genetics·2026

Frequent FBN2 variants in pectus excavatum highlight underlying phenotypic variability.

Journal of medical genetics·2026

Longest surviving patient with a homozygous splice-altering EGFR pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.

Journal of medical genetics·2026

Functional characterisation and pathological significance of variants of MEF2C promoter in tetralogy of Fallot.

Journal of medical genetics·2026

Identification of biallelic loss-of-function PREP variants in three individuals with syndromic intellectual disability.

Journal of medical genetics·2026

Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.

Journal of medical genetics·2026

Healthcare professionals' perspectives and preferences regarding adolescent meningococcal disease vaccination in the United States.

Expert review of vaccines·2026

A Nationwide Review of the Utilization of Rapid Antigen Testing for Group A Streptococcus.

Cureus·2026

Homozygous familial hypercholesterolemia, experience with Evinacumab treatment in two Mexican pediatric patients: case report.

Frontiers in genetics·2026

Psychiatric and medical profiles of children receiving health protection measures in a tertiary care facility: A five-year analysis.

Dusunen adam : Bakirkoy Ruh ve Sinir Hastaliklari Hastanesi yayin organi·2026

Predictors of parental stress in families of children with neurodevelopmental disabilities.

Dusunen adam : Bakirkoy Ruh ve Sinir Hastaliklari Hastanesi yayin organi·2026

Venous malformation with localized intravascular coagulopathy in children treated with sclerotherapy and LWMH.

Frontiers in pediatrics·2026

Related Experiment Videos

The genetic testing of children

Related Concept Videos

The distribution of healthcare workforces relative to population ill health in England: Repeated cross-sectional analysis of Census data 2001-2021.

Prevalence of transthyretin cardiac amyloidosis in undifferentiated heart failure with preserved ejection fraction.

The inflexible mind: A critical factor in understanding and addressing COVID-19 vaccine hesitancy.

An outbreak of SARS-CoV-2 in a public-facing office in England.

Delayed tension pneumocephalus and pneumorrhacis after routine cervical spine surgery treated successfully without burr holes.

The relationship between parental adverse childhood experiences and the health, well-being and development outcomes of their children: a systematic review.

Cancer Variant Interpretation Group UK (CanVIG-UK): updates on an exemplar national subspecialty multidisciplinary network.

Frequent <i>FBN2</i> variants in pectus excavatum highlight underlying phenotypic variability.

Longest surviving patient with a homozygous splice-altering <i>EGFR</i> pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathy.

Functional characterisation and pathological significance of variants of <i>MEF2C</i> promoter in tetralogy of Fallot.

Identification of biallelic loss-of-function <i>PREP</i> variants in three individuals with syndromic intellectual disability.

Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.

Healthcare professionals' perspectives and preferences regarding adolescent meningococcal disease vaccination in the United States.

A Nationwide Review of the Utilization of Rapid Antigen Testing for Group A Streptococcus.

Homozygous familial hypercholesterolemia, experience with Evinacumab treatment in two Mexican pediatric patients: case report.

Psychiatric and medical profiles of children receiving health protection measures in a tertiary care facility: A five-year analysis.

Predictors of parental stress in families of children with neurodevelopmental disabilities.

Venous malformation with localized intravascular coagulopathy in children treated with sclerotherapy and LWMH.

Related Experiment Videos

The genetic testing of children

Related Concept Videos

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