13q22.1-q32.1 Microdeletion Syndrome
Indian J Pediatr
.
2019 Mar;86(3):303-305.
doi: 10.1007/s12098-018-2789-7.
Epub 2018 Nov 7.
Authors
Ming-Wei Li
1
2
,
Xin-Yi Zou
3
,
Chao-Chun Zou
4
Affiliations
1
Children's Hospital, Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310051, China.
2
Zhejiang University School of Medicine, Hangzhou, China.
3
School of Medicine of Zhejiang University City College, Hangzhou, China.
4
Children's Hospital, Zhejiang University School of Medicine, 3333 Binsheng Road, Hangzhou, 310051, China. zcc14@zju.edu.cn.
PMID:
30406597
DOI:
10.1007/s12098-018-2789-7
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Abnormalities, Multiple / genetics*
Child, Preschool
Choanal Atresia / genetics*
Chromosome Deletion*
Chromosomes, Human, Pair 13
Cisterna Magna / abnormalities*
Female
Humans
Male
Grants and funding
LR13H090002/Zhejiang Provincial Natural Science Foundation/International
2016/Zhejiang Provincial Program for the Cultivation of Hight-level Innovative Health Talents/International