Documents (787) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	3524231	Treatment of Duchenne muscular dystrophy with growth hormone inhibitors. A controlled, double-blind	1.04 KB	2015-11-27	16	7	-
PubMed	10330430	Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy. We identified t	1.03 KB	2015-11-15	11	6	-
PubMed	10480348	Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dy	1.77 KB	2015-11-15	10	11	-
PubMed	2927388	Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptib	1.74 KB	2015-12-04	9	4	-
PubMed	9620771	Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations	1.6 KB	2015-11-27	25	11	-
PubMed	2390095	Total deficiency of plasma cholesteryl ester transfer protein in subjects homozygous and heterozygou	1.26 KB	2015-03-12	8	5	-
PubMed	8968716	BRCA1 R841W: a strong candidate for a common mutation with moderate phenotype. BRCA1 mutations cause	1.53 KB	2015-11-27	27	10	-
PubMed	133535	Linkage of gene for C2 deficiency and the major histocompatibility complex MHC in man. Family study	731 Bytes	2015-11-22	10	6	-
PubMed	1999552	Hereditary deficiency of C5 in association with discoid lupus erythematosus. A 29-year-old woman wit	405 Bytes	2015-12-07	14	7	-
PubMed	9020847	Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice. Myotonic d	1.16 KB	2015-11-27	26	4	-