Neurology Specific Literature Search   
 
[home][thesaurus]
    
Click Here to return To Results

 

Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993
See this aricle in Pubmed

Article Abstract
Molecular cytogenetic technology should be used in cases of suspected Miller-Dieker syndrome when high-resolution cytogenetic analysis fails to detect del(17)(p13.3).Positive findings should be followed up with parental studies.In addition,omphalocele should be included among the list of malformations that make up the Miller-Dieker syndrome.
 
Related Tags
(click to filter results - removes previous filter)

chromosomal abnormality
congenital malformation
gene
in situ hybridization
lissencephaly
malformation,CNS,congenital
microcephaly
Miller-Dieker syndrome
molecular genetics
omphalocele
prenatal diagnosis by amniocentesis

Click Here to return To Results