TEST-DiseaseOrPhenotypicFeature  

Documents (100) JSON TSV

source DB source ID text size updated at # proj. # Ann. updated_at
PubMed 14510914 Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein. OBJECTIVE: I 1.88 KB 2015-11-18 15 5 2021-12-23
PubMed 15041272 A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. Clinical, l 1.53 KB 2015-11-18 19 8 2021-12-23
PubMed 15096016 Pallidal stimulation: an alternative to pallidotomy? A resurgence of interest in the surgical treatm 1.33 KB 2021-12-23 8 9 2021-12-23
PubMed 15099351 Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia. Prop 1.09 KB 2015-11-18 12 6 2021-12-23
PubMed 15122708 Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotei 1.53 KB 2015-11-18 11 15 2021-12-23
PubMed 15188772 Severe reversible left ventricular systolic and diastolic dysfunction due to accidental iatrogenic e 830 Bytes 2017-09-04 10 2 2021-12-23
PubMed 15614572 Effects of the antidepressant trazodone, a 5-HT 2A/2C receptor antagonist, on dopamine-dependent beh 1.92 KB 2015-11-22 8 7 2021-12-23
PubMed 15623763 TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients. PURPOSE: T 1.89 KB 2015-11-18 13 4 2021-12-23
PubMed 15818664 Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslate 2.28 KB 2015-11-19 11 13 2021-12-23
PubMed 15824163 No Evidence for BRAF as a melanoma/nevus susceptibility gene. Somatic mutations of BRAF have been id 1.75 KB 2015-11-19 12 14 2021-12-23