Documents (787) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	6859721	Absence of the seventh component of complement in a patient with chronic meningococcemia presenting	662 Bytes	2015-12-06	6	12	-
PubMed	10071185	Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency. Dihydropyrimidin	1.27 KB	2015-11-02	3	11	-
PubMed	1323345	Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amp	1.4 KB	2015-11-18	5	5	-
PubMed	2828430	Homozygous hypobetalipoproteinemia: a disease distinct from abetalipoproproteinemia at the molecular	1.13 KB	2015-11-27	12	9	-
PubMed	10471457	A population-based study of the clinical expression of the hemochromatosis gene. BACKGROUND AND METH	2.3 KB	2015-11-15	5	14	-
PubMed	9949209	Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a regi	1.49 KB	2015-11-27	3	17	-
PubMed	7574457	Overexpression of DM20 messenger RNA in two brothers with Pelizaeus-Merzbacher disease. Pelizaeus-Me	1.4 KB	2015-11-27	2	6	-
PubMed	8808605	Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for gluco	1.49 KB	2015-11-27	3	5	-
PubMed	10466420	Homozygosity for a novel DTDST mutation in a child with a 'broad bone-platyspondylic' variant of dia	756 Bytes	2015-11-15	12	5	-
PubMed	1676565	Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anon	706 Bytes	2015-11-23	4	4	-