SMC2: a candidate gene associated with Cornelia de Lange Syndrome

ABSTRACT: whole-genome aCGH analysis also showed us that the patient carried a 12.01-1M Mb deletion region at chromosome bands 9q31.1-q32 (105,190,105-117,195,154). The deleted region encompasses 22 genes including SMC2 Two-condition Samples, Cornelia de Lange Syndrome vs. Normal cells.

ORGANISM(S): Homo sapiens

SUBMITTER: wang liang 

PROVIDER: E-GEOD-54354 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress