<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2025</volume><submitter>Khan T</submitter><funding>Stanley Manne Children's Research Institute, Ann &amp; Robert H. Lurie Children's Hospital of Chicago</funding><journal>Human mutation</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12373473</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz–Jeghers Syndrome</pubmed_title><pmcid>PMC12373473</pmcid><pubmed_authors>Yap K</pubmed_authors><pubmed_authors>Malik N</pubmed_authors><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Tariq M</pubmed_authors><pubmed_authors>Davis E</pubmed_authors><pubmed_authors>Satti H</pubmed_authors><pubmed_authors>Khan A</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Khan T</pubmed_authors><pubmed_authors>Safeer M</pubmed_authors><pubmed_authors>Khan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz–Jeghers Syndrome</name><description/><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-04-08T09:13:15.968Z</modification><creation>2026-04-08T00:47:47.209Z</creation></dates><accession>S-EPMC12373473</accession><cross_references/></HashMap>