Pages that link to "Q72090621"

The following pages link to Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm (Q72090621):

Displaying 18 items.

• Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse (Q22003952) ‎ (← links)
• Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organelles (Q24317236) ‎ (← links)
• Molecular cloning and characterization of rab27a and rab27b, novel human rab proteins shared by melanocytes and platelets (Q24336677) ‎ (← links)
• Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity (Q24538795) ‎ (← links)
• The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation (Q24597752) ‎ (← links)
• A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2 (Q24671618) ‎ (← links)
• Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding time (Q28507527) ‎ (← links)
• A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice (Q28584940) ‎ (← links)
• Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6 (Q28585075) ‎ (← links)
• The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome (Q36560640) ‎ (← links)
• A fusion pore phenotype in mast cells of the ruby-eye mouse (Q37036200) ‎ (← links)
• Lung disease in mice with cystic fibrosis (Q37376391) ‎ (← links)
• Pigmentation, pleiotropy, and genetic pathways in humans and mice (Q42950853) ‎ (← links)
• High-resolution genetic mapping of the gunmetal gene which regulates platelet production (Q48065788) ‎ (← links)
• Mart1 is located on mouse chromosome 19 and is excluded as a candidate for ep and ru (Q57281789) ‎ (← links)
• PCR-analyzed microsatellites for the inbred mouse strain 129/Sv, the strain most commonly used in gene knockout technology (Q71184181) ‎ (← links)
• Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD) (Q72160523) ‎ (← links)
• rim2 (recombination-induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak syndrome (HPS): genetic and physical mapping (Q74063817) ‎ (← links)