Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence.

Pilz, D T

Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence. [electronic resource] - Genetics in medicine : official journal of the American College of Medical Genetics - 29-33 p. digital

Publication Type: Journal Article

1098-3600

10.1097/00125817-199811000-00007 doi


1-Alkyl-2-acetylglycerophosphocholine Esterase
Brain--abnormalities
Chromosomes, Human, Pair 17
Female
Gene Deletion
Genetic Markers
Humans
In Situ Hybridization, Fluorescence
Male
Microtubule-Associated Proteins--genetics
Mutation