Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by F Katz
Trisomy X in a Female Member of a Family With X Linked Severe Combined Immunodeficiency: Implications for Carrier Diagnosis.
Journal of Medical Genetics
Genetics
Related publications
A Novel X-Linked Combined Immunodeficiency Disease.
Journal of Clinical Investigation
Medicine
Preclinical Development of Gene Therapy for X-Linked Severe Combined Immunodeficiency (SCID-X1)
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Rat Polyomavirus 2 Infection in a Colony of X-Linked Severe Combined Immunodeficiency Rats in Japan
Journal of Veterinary Medical Science
Veterinary
Characterization of an MDR1 Retroviral Bicistronic Vector for Correction of X-Linked Severe Combined Immunodeficiency
Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Severe Manifestations in Carrier Females in X Linked Retinitis Pigmentosa.
Journal of Medical Genetics
Genetics
Diagnosis of Severe Combined Immunodeficiency
Journal of Clinical Pathology
Medicine
Forensic Medicine
Pathology
Defective Human Interleukin 2 Receptor Gamma Chain in an Atypical X Chromosome-Linked Severe Combined Immunodeficiency With Peripheral T Cells.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Novel Mutation in a Kazakh Family With X-Linked Alport Syndrome
PLoS ONE
Multidisciplinary
Shared Gamma(c) Subunit Within the Human Interleukin-7 Receptor Complex. A Molecular Basis for the Pathogenesis of X-Linked Severe Combined Immunodeficiency.
Journal of Clinical Investigation
Medicine