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Blood Advances
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September 26, 2025
Reading between the (long) lines: one-stop F8 gene analysis?
Julie A Majerus, Juliana Perez Botero
Seminars in Thrombosis and Hemostasis
|
September 15, 2017
Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience
Juliana Perez Botero, Lea M Coon, Julie A Majerus, et al.
American Journal of Clinical Pathology
|
May 5, 2017
Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden: A Comparison of Institutional and National Provider Practices
Juliana Perez Botero, Julie A Majerus, Ann K Strege, et al.
American Journal of Clinical Pathology
|
November 26, 2025
Distinct clinical, laboratory, molecular, and pathologic features of systemic mastocytosis involving the gastrointestinal tract
April Chiu, David S Viswanatha, Rong He, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
August 26, 2006
BRAF mutation analysis in fine needle aspiration (FNA) cytology of the thyroid
Long Jin, Thomas J Sebo, Nobuki Nakamura, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
September 9, 2016
Practice patterns in the diagnosis of inherited platelet disorders within a single institution
Juliana Perez Botero, Rajiv K Pruthi, Julie A Majerus, et al.
Platelets
|
November 2, 2017
Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype
Juliana Perez Botero, Dong Chen, Julie A Majerus, et al.
Leukemia & Lymphoma
|
December 10, 2016
Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia
Juliana Perez Botero, Dong Chen, Margot A Cousin, et al.
Platelets
|
April 29, 2016
Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family
Juliana Perez Botero, Dong Chen, Rong He, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2018
Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant
Chen G Han, Kevin J O'Brien, Lea M Coon, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Blood Advances
|
September 26, 2025
Reading between the (long) lines: one-stop F8 gene analysis?
Julie A Majerus, Juliana Perez Botero
Seminars in Thrombosis and Hemostasis
|
September 15, 2017
Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience
Juliana Perez Botero, Lea M Coon, Julie A Majerus, et al.
American Journal of Clinical Pathology
|
May 5, 2017
Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden: A Comparison of Institutional and National Provider Practices
Juliana Perez Botero, Julie A Majerus, Ann K Strege, et al.
American Journal of Clinical Pathology
|
November 26, 2025
Distinct clinical, laboratory, molecular, and pathologic features of systemic mastocytosis involving the gastrointestinal tract
April Chiu, David S Viswanatha, Rong He, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
August 26, 2006
BRAF mutation analysis in fine needle aspiration (FNA) cytology of the thyroid
Long Jin, Thomas J Sebo, Nobuki Nakamura, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
September 9, 2016
Practice patterns in the diagnosis of inherited platelet disorders within a single institution
Juliana Perez Botero, Rajiv K Pruthi, Julie A Majerus, et al.
Platelets
|
November 2, 2017
Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype
Juliana Perez Botero, Dong Chen, Julie A Majerus, et al.
Leukemia & Lymphoma
|
December 10, 2016
Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia
Juliana Perez Botero, Dong Chen, Margot A Cousin, et al.
Platelets
|
April 29, 2016
Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family
Juliana Perez Botero, Dong Chen, Rong He, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2018
Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant
Chen G Han, Kevin J O'Brien, Lea M Coon, et al.
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of 1