High frequency of genomic deletions - and a duplication - in the LIS1 gene in lissencephaly: implications for molecular diagnosis

Subjects

Subjects :

Encephalopathy -- Diagnosis
Encephalopathy -- Genetic aspects
Encephalopathy -- Research
Gene mutations -- Analysis
Nucleotide sequencing -- Usage
Polymerase chain reaction -- Usage
Health

Details

Language :

English

ISSN :

00222593

Volume :

45

Issue :

6

Database :

Gale General OneFile

Journal :

Journal of Medical Genetics

Publication Type :

Periodical

Accession number :

edsgcl.180833829