<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE300nnn/GSE300874/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type> SNP genotyping by SNP array</gds_type><gds_type>Genome variation profiling by SNP array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE300874</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Genetic diagnosis of 5 patients in a consanguineous family</name><description>Rare disease loci is searched via linkage mapping using these SNP markers.</description><dates><publication>2026/07/01</publication></dates><accession>GSE300874</accession><cross_references><GSM>GSM9070300</GSM><GSM>GSM9070301</GSM><GSM>GSM9070298</GSM><GSM>GSM9070299</GSM><GSM>GSM9070302</GSM><GSM>GSM9070296</GSM><GSM>GSM9070297</GSM><GPL>28939</GPL><GPL>21168</GPL><GSE>300874</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>