Related Experiment Videos
Heterotaxia syndromes and 22q11 deletion
Journal of Medical Genetics
|December 1, 1996
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Neural Stimulation Hardware for the Selective Intrafascicular Modulation of the Vagus Nerve.
IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society·2023
Decoding bladder state from pudendal intraneural signals in pigs.
APL bioengineering·2023
Deletion of the SHOX gene in patients with short stature of unknown cause.
American journal of medical genetics. Part A·2003
Two novel mutations of the human delta7-sterol reductase (DHCR7) gene in children with Smith-Lemli-Opitz syndrome.
Molecular and cellular probes·2002
Exploring the clinical and mutational spectrum of MORC2-associated disorders.
Journal of medical genetics·2026
Founder variant in OTOG causing non-syndromic sensorineural hearing loss in Irish traveller population.
Journal of medical genetics·2026
Risk of breast cancer after ovarian cancer in germline BRCA1/2 heterozygotes.
Journal of medical genetics·2026
Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.
Journal of medical genetics·2026
Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.
Journal of medical genetics·2026
Novel MORC2 variants in Charcot-Marie-Tooth disease type 2Z: genetic and functional insights.
Frontiers in medicine·2026
[Exogenous ochronosis: An underdiagnosed cause of acquired facial hyperpigmentation].
Annales de pathologie·2026
Abdominal aortic aneurysm in a patient with situs ambiguous and polyspleny (heterotaxy syndrome): a very rare occurrence in vascular surgery! Short literature review.
Surgical and radiologic anatomy : SRA·2026
Congenital anosmia.
Danish medical journal·2026