Related Experiment Videos
Congenital hypothyroidism and hyperthyroidism in monozygotic twin girls
Journal of Medical Genetics
|December 1, 1971
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats.
American journal of human genetics·1999
Cardiomyopathy of limb-girdle muscular dystrophy.
Journal of the American College of Cardiology·1994
Tetrasomy 21 in megakaryoblastic leukemia.
Cancer genetics and cytogenetics·1994
Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.
Journal of medical genetics·2026
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
Double Layered Breathable Knitted Fabric With Human Motion Adaptive Function for the Dynamic Thermal Management.
Small (Weinheim an der Bergstrasse, Germany)·2026
Structural origins of species-specific differences in TRPV2 activation.
Nature communications·2026
Sex differences in ex vivo cytokine production and their association with outcome following ischemic stroke.
Frontiers in immunology·2026
Loading conditions rather than contractility primarily determine biventricular ejection fraction in endotoxic shock.
American journal of physiology. Heart and circulatory physiology·2026