Home LiteratureArticle Details
PMID: 3004790 Published · ppublish English Case Reports Letter

Inherited Xp21 deletion in a boy with complex glycerol kinase deficiency syndrome.

Clinical genetics ·Vol. 29 ·No. 1 ·1986-01-00 ·Pages 92-3

Saito F, Goto J, Kakinuma H, Nakamura F, Murayama S, Nakano I, Tonomura A

Abstract

暂无摘要

MeSH Terms
Child Chromosome Deletion Female Glycerol Kinase/deficiency Humans Male Ornithine Carbamoyltransferase Deficiency Disease Phosphotransferases/deficiency Sex Chromosome Aberrations X Chromosome
Chemicals
Phosphotransferases Glycerol Kinase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Saito F
Goto J
Kakinuma H
Nakamura F
Murayama S
Nakano I
Tonomura A
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
DOI
10.1111/j.1399-0004.1986.tb00777.x
Published
1986-01-00
Pages
92-3
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
External Links
PubMed source DOI: 10.1111/j.1399-0004.1986.tb00777.x View journal details
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com

Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2