Related Experiment Videos
Expression of fragile site at 10q25 in normal culture conditions
American Journal of Human Genetics
|January 1, 1983
Abstract
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
Genetic data sharing by clinical laboratories in Canada: A position statement by the Canadian College of Medical Geneticists.
American journal of human genetics·2026
Robust cis-by-trans epistasis in the human plasma proteome highlights an ABO-centered interaction network.
American journal of human genetics·2026
International experiences of genomic newborn screening: Lessons from over 10,800 newborns.
American journal of human genetics·2026
A rare recurring gain-of-function variant in BMPR2 causes neurodevelopmental phenotypes in humans and flies.
American journal of human genetics·2026
A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity.
American journal of human genetics·2026
CanVar-UK: A collaborative platform for germline interpretation in cancer susceptibility genes.
American journal of human genetics·2026