Documents (100) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	8931695	Phenotypic and genotypic overlap between atelosteogenesis type 2 and diastrophic dysplasia. Mutation	1.82 KB	2015-11-27	35	18	-
PubMed	8640236	Low incidence of BRCA2 mutations in breast carcinoma and other cancers. Inherited mutant alleles of	1.47 KB	2015-11-27	26	17	-
PubMed	8954016	Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartom	2.01 KB	2015-11-27	33	17	-
PubMed	9145677	BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer. BACKGROUND: To d	1.84 KB	2015-11-28	24	14	-
PubMed	8644702	Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden. Nine different	1.86 KB	2015-11-27	27	13	-
PubMed	8929264	The DCC protein and prognosis in colorectal cancer. BACKGROUND: Allelic loss of chromosome 18q predi	1.5 KB	2015-12-06	24	13	-
PubMed	8894695	HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome. Complete hypoxanthine-guanine pho	1.2 KB	2015-12-06	24	13	-
PubMed	8968760	Ataxia-telangiectasia: founder effect among north African Jews. The ATM gene is responsible for the	1.11 KB	2015-11-27	26	12	-
PubMed	9090524	A clinical overview of WT1 gene mutations. Mutations in the WT1 gene were anticipated to explain the	694 Bytes	2015-12-08	24	11	-
PubMed	8589723	Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNT	1.48 KB	2015-11-27	25	11	-