Concepedia

Maternal origin of inv dup(15) chromosomes in infantile autism

Tommy Martinsson, Tonnie Johannesson, Mihailo Vujic, A. Sj�stedt, Suzanne Steffenburg, J. Wahlstr�m

European Child & Adolescent Psychiatry · 1996 · 54 citations · 27 references

Concepts

Life SciencesGeneticsMolecular GeneticsAutism Spectrum DisordersCytogeneticsHuman GeneticsAneuploidyAutism Spectrum Disorder GeneticsCopy Number VariantsNeurodevelopmental DisordersNeurodevelopmental GeneticsNeurogenetic DisordersAneuploidy In Developmental DisordersAutism Spectrum Disorder Copy Number VariantsCopy Number Variations In Developmental DisordersDevelopmental Delay Copy Number VariantsNeurodevelopmental Copy Number Variants

References

27

Diagnostic and Statistical Manual of Mental Disorders

&NA; · Alzheimer Disease & Associated Disorders · 1988 · 12.7K citations

Medicine, Pediatrics, Psychiatry +4

The American Journal of Human Genetics

J. S. · Population · 1950 · 5.1K citations

Life Sciences, Biology, Genetics +4

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 887 citations

Life Sciences, Genetics, Molecular Genetics +11

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

Joan H.M. Knoll, Robert D. Nicholls, R.E. Magenis et al. · American Journal of Medical Genetics · 1989 · 583 citations

Life Sciences, Genetics, Molecular Genetics +17

Uniparental paternal disomy in Angelman's syndrome

S Malcolm, Jill Clayton‐Smith, M. Nichols et al. · The Lancet · 1991 · 330 citations

Life Sciences, Genetics, Cytogenetics +6