Home LiteratureArticle Details
PMID: 7530551 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

A de novo deletion in FMR1 in a patient with developmental delay.

Human molecular genetics ·Vol. 3 ·No. 9 ·1994-09-00 ·Pages 1705-6

Gu Y, Lugenbeel KA, Vockley JG, Grody WW, Nelson DL

Abstract

暂无摘要

Related Genes
FMR1
MeSH Terms
Base Sequence Chromosome Mapping DNA Primers/genetics Developmental Disabilities/genetics Female Fragile X Syndrome/genetics Germ-Line Mutation Humans Infant Male Molecular Sequence Data Oligodeoxyribonucleotides/genetics Phenotype Polymerase Chain Reaction Repetitive Sequences, Nucleic Acid Sequence Deletion
Chemicals
DNA Primers Oligodeoxyribonucleotides
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Gu Y
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030.
Lugenbeel K A
Vockley J G
Grody W W
Nelson D L
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
DOI
10.1093/hmg/3.9.1705
Published
1994-09-00
Pages
1705-6
Language
English
Region
England
NLM ID
9208958
Subset
IM
Grants
NICHD NIH HHS · HD29256 · United States
Databases
GENBANK
L29074
External Links
PubMed source DOI: 10.1093/hmg/3.9.1705 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