Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect

Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect

<p>Abstract</p> <p>Background</p> <p>Recent development of MLPA (Multiplex-Ligation-dependent Probe Amplification, MRC-Holland) and microarray technology allows detection of a wide range of new submicroscopic abnormalities. Publishing new cases and case reviews associat...

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Bibliographic Details
Main Authors: Srebniak Malgorzata I, Boter Marjan, Verboven-Peerden Carla MA, Looye-Bruinsma Gerda AG, Oudesluijs Gretel, Galjaard Robert-Jan H, Van Opstal Diane
Format: Article
Language:English
Published: BMC 2011-12-01
Series:Molecular Cytogenetics
Subjects:
18p11.32 deletion
18p11.32 duplication
submicroscopic abnormality
normal phenotype
MLPA
SNP array
Online Access:http://www.molecularcytogenetics.org/content/4/1/27

Internet

http://www.molecularcytogenetics.org/content/4/1/27

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