The KBG syndrome: Confirmation of autosomal dominant inheritance and further delineation of the phenotype
Year: 2004
Type: article
Study design: Case Report
DOI: 10.1002/ajmg.a.30291
Institution: Ankara University
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2029420107
