Related Experiment Video
Updated: Oct 15, 2026

05:51
A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3
H S Scott1, S E Antonarakis, L Mittaz
1Division of Medical Genetics, University of Geneva Medical School, Switzerland. Hamish.Scott@medecine.unige.ch
Advances in Oto-Rhino-Laryngology
|June 27, 2000
Abstract
No abstract available in PubMed .
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