biored-valid

Documents (39) 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	30	37	-
PubMed	15018851	Comparison of sequential cytomegalovirus isolates in a patient with lymphoma and failing antiviral t	1.61 KB	2015-11-22	40	30	-
PubMed	15041272	A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. Clinical, l	1.53 KB	2015-11-18	34	31	-
PubMed	15069170	Four novel mutations in the thiazide-sensitive Na-Cl co-transporter gene in Japanese patients with G	1.81 KB	2015-11-22	41	46	-
PubMed	15086325	Identification of three F5 gene mutations associated with inherited coagulation factor V deficiency	1.38 KB	2015-11-22	40	20	-
PubMed	15096016	Pallidal stimulation: an alternative to pallidotomy? A resurgence of interest in the surgical treatm	1.33 KB	2021-12-23	24	14	-
PubMed	15579441	Hypoxia in renal disease with proteinuria and/or glomerular hypertension. Despite the increasing nee	1.47 KB	2015-11-22	57	25	-
PubMed	15754732	Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with cli	1.92 KB	2015-11-19	43	36	-
PubMed	15867855	Genetic variants of the T-cell immunoglobulin mucin 1 but not the T-cell immunoglobulin mucin 3 gene	1.71 KB	2025-10-02	46	26	-
PubMed	15951966	Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH. BACKGROUND: Exonic deletions in	1.35 KB	2015-11-19	42	17	-