Related Experiment Videos
Frequency and predictive value of 22q11 deletion
Journal of Medical Genetics
|October 21, 1999
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Impact of COVID-19 on management and outcomes of NHS patients with recurrent respiratory papillomatosis: evidence from a UK registry.
Annals of the Royal College of Surgeons of England·2025
European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender.
The British journal of surgery·2021
Meeting report from the joint IARC-NCI international cancer seminar series: a focus on colorectal cancer.
Annals of oncology : official journal of the European Society for Medical Oncology·2019
Estimates of benefits and harms of prophylactic use of aspirin in the general population.
Annals of oncology : official journal of the European Society for Medical Oncology·2014
A preliminary genetic map in Solea senegalensis (Pleuronectiformes, Soleidae) using BAC-FISH and next-generation sequencing.
Cytogenetic and genome research·2013
CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.
Journal of medical genetics·2026
Single-cell transcriptomics identifies neural fate disruption and glial reprogramming caused by RARS2 deficiency.
Journal of medical genetics·2026
Unified genetic risk score for prostate cancer enables improved risk stratification for clinical decision-making.
Journal of medical genetics·2026
Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.
Acta crystallographica. Section F, Structural biology communications·2026
Dopamine Receptor D2 gene Polymorphisms rs2005313, rs4274224, and rs4938019 in Pakistani Patients with Schizophrenia:a Diagnostic Tool for Schizophrenia.
Journal of molecular neuroscience : MN·2026
Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.
Clinical endocrinology·2026
CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.
European journal of endocrinology·2026
Integrating Brain Morphological Features and Ionized Serum Magnesium to Identify Mild Tic Comorbidity in Children with Autism Spectrum Disorder.
Neuropsychiatric disease and treatment·2026