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Publications by Nivedita U. Jerath
Coexistence of a T118MPMP22missense Mutation and Chromosome 17 (17p11.2-P12) Deletion
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
Resolving a Multi-Generational Neuromuscular Mystery in a Family Presenting With a Variable Scapuloperoneal Syndrome in a C.464G>A, p.Arg155His VCP Mutation
Case Reports in Genetics
Related publications
Identification of Novel Candidate Oncogenes in Chromosome Region 17p11.2-P12 in Human Osteosarcoma
PLoS ONE
Multidisciplinary
Molecular Characterisation of a Proximal Chromosome 18q Deletion
Journal of Medical Genetics
Genetics
Molecular Analysis of a Deletion Polymorphism in Alpha Satellite of Human Chromosome 17: Evidence for Homologous Unequal Crossing-Over and Subsequent Fixation
Nucleic Acids Research
Genetics
A Calmodulin Pseudogene on Human Chromosome 17
Nucleic Acids Research
Genetics
Chromosome 3q29 Deletion With Gastrointestinal Malformation: A Case Report
Journal of Medical Case Reports
Medicine
Clinical and Neurophysiological Features of the Hereditary Neuropathy With Liability to Pressure Palsy Due to the 17p11.2 Deletion
Arquivos de Neuro-Psiquiatria
Biological Psychiatry
Neurology
Deletion of Chromosome 2 (P11-P13): Case Report and Review.
Journal of Medical Genetics
Genetics
Deletion Mapping of Chromosome 16q in Hepatocellular Carcinoma
British Journal of Cancer
Cancer Research
Oncology
Chromosome 10q26 Deletion Syndrome: Two New Cases and a Review of the Literature
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
