Work

Kagami–Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3

Year: 2020

Type: article

Study design: Case Report

Source: Journal of Human Genetics

DOI: 10.1038/s10038-020-00858-x

Authors: Jessica Omark, Yohei Masunaga, Mark Hannibal, Brandon Shaw, Maki Fukami, Fumiko Kato, Hirotomo Saitsu, Masayo Kagami, Tsutomu Ogata

Institutions: University of Michigan, Hamamatsu University School of Medicine, Henry Ford Health, Henry Ford Hospital, National Research Institute for Child Health and Development

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Japan Society for the Promotion of Science

Awards: G5138091885, Clarification of underlying factors for disorders of sex development and reproductive dysfunction as multifactorial disorders

OpenAlex ID: W3093273774

FWCI: 0.146

Cites: 10

Cited by: 1

Related to: 10