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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations

PaperCitations, authors & open-access status

Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 104 citations, 2014 year and bronze oa status.

104
Citations
2014
Year
bronze
OA Status

Related on ScholarIQ

Thomas J. J. Maal
Author
European Journal of Human Genetics
Journal
Genomics and Rare Diseases
Topic
Genomics and Rare Diseases
Topic
Genetics and Neurodevelopmental Disorders
Topic
Genomic variations and chromosomal abnormalities
Topic
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