Documents (100) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	9831355	I1307K APC and hMLH1 mutations in a non-Jewish family with hereditary non-polyposis colorectal cance	629 Bytes	2015-11-27	27	5	-
PubMed	9843038	Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family. H	971 Bytes	2015-11-27	26	4	-
PubMed	9848786	Human complement factor H deficiency associated with hemolytic uremic syndrome. This study reports o	1.04 KB	2015-11-27	28	12	-
PubMed	9852676	Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibr	1.25 KB	2015-03-12	23	10	-
PubMed	9856498	The molecular basis of C6 deficiency in the western Cape, South Africa. Deficiency of the sixth comp	1.22 KB	2015-03-12	23	7	-
PubMed	9856499	Complement C7 deficiency: seven further molecular defects and their associated marker haplotypes. Se	513 Bytes	2015-03-12	23	4	-
PubMed	9861003	A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk	1.49 KB	2015-03-12	23	10	-
PubMed	9863607	Segregation distortion in myotonic dystrophy. Myotonic dystrophy (DM) is an autosomal dominant disea	1.09 KB	2015-11-28	25	14	-
PubMed	9867744	Diagnosis of hemochromatosis. If untreated, hemochromatosis can cause serious illness and early deat	1.03 KB	2015-11-27	25	7	-
PubMed	9869602	Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for co	1.38 KB	2015-11-28	26	13	-