GEOapplication/xmlftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE296nnn/GSE296489/primaryOK200GenomicsHomo sapiens SNP genotyping by SNP arrayGenome variation profiling by SNP arrayhttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE296489GEOGSEfalseClinical Phenotype and Genetic Analysis of a Family with 17q12 Microdeletion SyndromeTo clarify the genetic etiology of a 17q12 microdeletion syndrome fetus in a family and analyze the correlation between the genetic and clinical phenotypes within the family. The child and her father, who share the same genetic variation, exhibit significant clinical heterogeneity.2026/05/07GSE296489GSM8971576GSM8971577GSM8971578GSM897157918637296489Homo sapiens