Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky–Pudlak syndrome: role of insC974 in platelet function and clinical …
R González‐Conejero, J Rivera… - British journal of …, 2003 - Wiley Online Library
Hermansky–Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which is
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky–Pudlak syndrome: role of insC974 in platelet function and clinical …
R Gonzalez-Conejero, J Rivera… - British Journal of …, 2003 - search.ebscohost.com
Hermansky–Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which is
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
[引用][C] Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky-Pudlak syndrome: role of insC9 74 in platelet function and clinical …
R GONZALEZ-CONEJERO, J RIVERA… - British journal of …, 2003 - pascal-francis.inist.fr
Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky-Pudlak
syndrome: role of insC9 74 in platelet function and clinical relevance CNRS Inist Pascal-Francis …
syndrome: role of insC9 74 in platelet function and clinical relevance CNRS Inist Pascal-Francis …
Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky-Pudlak syndrome: role of insC974 in platelet function and clinical …
R González-Conejero, J Rivera… - British journal of …, 2003 - pubmed.ncbi.nlm.nih.gov
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which is
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky-Pudlak syndrome: role of insC974 in platelet function and clinical …
R González-Conejero, J Rivera, G Escolar… - British Journal of …, 2003 - europepmc.org
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which is
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
[PDF][PDF] Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky–Pudlak syndrome: role of insC974 in platelet function and clinical …
J Corral - British Journal of Haematology, 2003 - academia.edu
Hermansky–Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which is
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky-Pudlak syndrome: role of insC974 in platelet function and clinical …
R Gonzalez-Conejero, J Rivera, G Escolar… - British Journal of …, 2003 - elibrary.ru
Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder, which is
genetically heterogeneous. In humans, mutations associated with this syndrome have been …
genetically heterogeneous. In humans, mutations associated with this syndrome have been …