Documents (100) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
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	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	2021-12-23
PubMed	15188772	Severe reversible left ventricular systolic and diastolic dysfunction due to accidental iatrogenic e	830 Bytes	2017-09-04	10	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	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	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	2021-12-23
PubMed	17962394	Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutat	1.3 KB	2015-11-23	13	2021-12-23
PubMed	16001362	An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nuc	2.06 KB	2015-11-19	12	2021-12-23
PubMed	16321363	Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation. We describ	925 Bytes	2015-11-23	16	2021-12-23
PubMed	16330669	Array-based comparative genomic hybridization analysis reveals recurrent chromosomal alterations and	2 KB	2015-11-19	12	2021-12-23