Developmental delay and dysmorphic features in a girl with a de novo 5.4 Mb deletion of 13q12.11-q12.13
Congenit Anom (Kyoto)
.
2020 Mar;60(2):73-74.
doi: 10.1111/cga.12346.
Epub 2019 Jun 27.
Authors
Makiko Tominaga
1
2
,
Toshiyuki Saito
3
,
Mitsuo Masuno
4
,
You Umeda
2
,
Kenji Kurosawa
1
Affiliations
1
Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
2
Children's Medical Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
3
Department of Clinical Laboratory, Kanagawa Children's Medical Center, Yokohama, Japan.
4
Genetic Counseling Program, Graduate School of Health and Welfare, Kawasaki University of Medical Welfare, Kurashiki, Japan.
PMID:
31206199
DOI:
10.1111/cga.12346
No abstract available
Grants and funding
Ministry of Health, Labour and Welfare, Japan
17K10069/JSPS KAKENHI