<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>87(6)</volume><submitter>Cabrera-Salcedo C</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development</funding><funding>NCATS NIH HHS</funding><funding>NICHD NIH HHS</funding><funding>National Institutes of Health</funding><journal>Clinical endocrinology</journal><pagination>874-876</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5698139</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Isolated growth hormone deficiency due to the R183H mutation in GH1: Clinical analysis of a four-generation family.</pubmed_title><pmcid>PMC5698139</pmcid><funding_grant_id>K23HD07335</funding_grant_id><funding_grant_id>UL1 TR001425</funding_grant_id><funding_grant_id>K23 HD073351</funding_grant_id><funding_grant_id>1UL1 TR001425</funding_grant_id><funding_grant_id>R01 HD078592</funding_grant_id><pubmed_authors>Shah AS</pubmed_authors><pubmed_authors>Hwa V</pubmed_authors><pubmed_authors>Tyzinski L</pubmed_authors><pubmed_authors>Backeljauw P</pubmed_authors><pubmed_authors>Cabrera-Salcedo C</pubmed_authors><pubmed_authors>Gutmark-Little I</pubmed_authors><pubmed_authors>Andrew M</pubmed_authors><pubmed_authors>Dauber A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Isolated growth hormone deficiency due to the R183H mutation in GH1: Clinical analysis of a four-generation family.</name><description/><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Dec</publication><modification>2025-04-05T10:32:18.518Z</modification><creation>2025-04-05T10:32:18.518Z</creation></dates><accession>S-EPMC5698139</accession><cross_references><pubmed>28626954</pubmed><doi>10.1111/cen.13400</doi></cross_references></HashMap>