Documents (500) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	19477219	Identified hidden genomic changes in mantle cell lymphoma using high-resolution single nucleotide po	1.85 KB	2015-11-25	5	0	-
PubMed	19110214	A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C	1.78 KB	2015-11-24	6	2	-
PubMed	18827003	A novel point mutation in the amino terminal domain of the human glucocorticoid receptor (hGR) gene	1.77 KB	2015-08-06	2	6	-
PubMed	18398821	Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expr	1.41 KB	2015-08-06	1	0	-
PubMed	18266724	Histamine-N-methyl transferase polymorphism and risk for migraine. BACKGROUND/OBJECTIVES: Histamine	1.14 KB	2015-11-24	3	2	-
PubMed	17437275	Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphou	1.13 KB	2015-11-23	5	0	-
PubMed	17003923	Gene polymorphisms implicated in influencing susceptibility to venous and arterial thromboembolism:	2.03 KB	2015-11-23	5	12	-
PubMed	16840830	Two novel mutations in the MEN1 gene in subjects with multiple endocrine neoplasia-1. Multiple endoc	1.34 KB	2015-11-23	26	2	-
PubMed	16288197	Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree. PURPOSE: C	2.59 KB	2015-11-19	29	4	-
PubMed	15353880	Fabry disease female proband with clinical manifestations similar to hypertrophic cardiomyopathy. Fa	1 KB	2015-11-22	8	0	-