Work

Clinical phenotype and candidate genes for the 5q31.3 microdeletion syndrome

Year: 2012

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.35439

Authors: Kana Hosoki, Tohru Ohta, Jun Natsume, Sumiko Imai, Akihisa Okumura, Takeshi Matsui, Naoki Harada, Carlos A. Bacino, Fernando Scaglia, Jeremy Y. Jones, Norio Niikawa, Shinji Saitoh

Institutions: Hokkaido University, Health Sciences University of Hokkaido, Nagoya University, Sagamino Hospital, Juntendo University, Mitsubishi Chemical (Japan), Baylor College of Medicine, Texas Children's Hospital, Nagoya City University

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2023017703

FWCI: 1.417

Cites: 11

Cited by: 32

Related to: 10