Documents (100) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
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	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	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
PubMed	16419642	A novel missense mutation, F826Y, in the mineralocorticoid receptor gene in Japanese hypertensives:	1.78 KB	2015-11-20	13	2021-12-23
PubMed	16629641	Definition and management of anemia in patients infected with hepatitis C virus. Chronic infection w	1.32 KB	2015-11-23	8	2021-12-23
PubMed	16731636	Enhanced isoproterenol-induced cardiac hypertrophy in transgenic rats with low brain angiotensinogen	1.47 KB	2015-11-23	8	2021-12-23
PubMed	16737910	Identification of the nuclear localization motif in the ETV6 (TEL) protein. ETV6, or Translocation-E	1.04 KB	2015-11-23	8	2021-12-23