Related Experiment Videos
Mucosal neuromata syndrome (MEN type IIb (III))
1Centre for Human Genetics, University of Leuven, Belgium.
Journal of Medical Genetics
|October 1, 1988
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence.
Journal of neurology, neurosurgery, and psychiatry·1995
Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS.
Journal of medical genetics·1995
Clinical profile of Angelman syndrome at different ages.
American journal of medical genetics·1995
Fragile X boys: evolution of the mental age in childhood. Preliminary data on 10 prepubertal boys.
Genetic counseling (Geneva, Switzerland)·1995
Costello syndrome: the natural history of a true postnatal growth retardation syndrome.
Genetic counseling (Geneva, Switzerland)·1995
Anal atresia and abdominal wall defect as unusual symptoms in EEC syndrome.
Genetic counseling (Geneva, Switzerland)·1995
Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank.
Journal of medical genetics·2026
Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.
Journal of medical genetics·2026
CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.
Journal of medical genetics·2026
Pediatric middle ear actinomycosis: report of two cases.
AME case reports·2026