Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics
PD Anderson, M Huizing, DA Claassen, J White… - Human genetics, 2003 - Springer
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics
PD Anderson, M Huizing, DA Claassen… - Human …, 2003 - pubmed.ncbi.nlm.nih.gov
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
Hermansky-Pudlak syndrome type4 (HPS-4): clinical and molecular characteristics
PD Anderson, M Huizing, DA Claassen, J White… - Human Genetics, 2003 - infona.pl
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics.
PD Anderson, M Huizing, DA Claassen, J White… - Human …, 2003 - europepmc.org
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics
PD Anderson, M Huizing, DA Claassen… - Human …, 2003 - search.proquest.com
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
[引用][C] Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics
PD ANDERSON, M HUIZING, DA CLAASSEN… - Human …, 2003 - pascal-francis.inist.fr
Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics CNRS
Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
[引用][C] Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics
A PD - Hum Genet, 2003 - cir.nii.ac.jp
Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics.
PD Anderson, M Huizing, DA Claassen… - Human …, 2003 - search.ebscohost.com
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
Hermansky-Pudlak syndrome type 4 (HPS-4): Clinical and molecular characteristics
PD Anderson, M Huizing… - Human …, 2003 - utsouthwestern.elsevierpure.com
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics
PD Anderson, M Huizing, DA Claassen, J White… - Human Genetics, 2003 - elibrary.ru
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder of oculocutaneous
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …
albinism and bleeding attributable to storage-pool-deficient platelets. Although at least 14 …