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Publications by J. Martin Johnston
MPP1/p55 Gene Deletion in a Hemophilia a Patient With Ectrodactyly and Severe Developmental Defects
American Journal of Hematology
Hematology
Related publications
Total C4B Deficiency Due to Gene Deletion and Gene Conversion in a Patient With Severe Infections
Clinical Diagnostic Laboratory Immunology
A 22q11.2 Deletion That Excludes UFD1L and CDC45L in a Patient With Conotruncal and Craniofacial Defects
American Journal of Human Genetics
Genetics
Second Case Report of Successful Electroconvulsive Therapy for a Patient With Schizophrenia and Severe Hemophilia A
Neuropsychiatric Disease and Treatment
Psychiatry
Mental Health
Biological Psychiatry
Hippocampal and Visuospatial Learning Defects in Mice With a Deletion of Frizzled 9, a Gene in the Williams Syndrome Deletion Interval
Development (Cambridge)
Developmental Biology
Molecular Biology
Targeted Deletion of the Mitogen-Activated Protein Kinase Kinase 4 Gene in the Nervous System Causes Severe Brain Developmental Defects and Premature Death
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Acquired Hemophilia a in a Patient With Advanced Prostate Cancer
Autopsy and Case Reports
Sixteen Novel Hemophilia a Causative Mutations in the First Argentinian Series of Severe Molecular Defects
Haematologica
Hematology
Acquired Hemophilia a in a Patient With Systemic Lupus Erythematosus.
Internal Medicine
Internal Medicine
Medicine
ssODN-mediated In-Frame Deletion With CRISPR/Cas9 to Restore the FVIII Function in Hemophilia a Patient-Derived iPSCs and ECs
Molecular Therapy - Nucleic Acids
Drug Discovery
Molecular Medicine
