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Publications by D Prabhu
Evaluation of DNA Damage and Mutation Screening of Exon 26 of SCN1A Gene in Patients With Epilepsy
International Journal of Epilepsy
Neurology
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Association Between SCN1A Gene Polymorphisms and Drug Resistant Epilepsy in Pediatric Patients
Seizure : the journal of the British Epilepsy Association
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Analysis of SCN1A Mutation and Parental Origin in Patients With Dravet Syndrome
Journal of Human Genetics
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Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment
Genetics Research International
Genetics
Molecular Biology
Mutation in Exon 13 of the TCOF1 Gene in Patient With Treacher Collins Syndrome
Acta Fytotechnica et Zootechnica
Animal Science
Zoology
Agronomy
Crop Science
Food Science
Screening of the Connexin 26 (35delg) Mutation in Egyptian Patients With Autosomal Recessive Nonsyndromic Deafness and Its Relation to the Patients' Iq
Egyptian Journal of Genetics and Cytology
De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
American Journal of Human Genetics
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Gene Promoter and Exon DNA Methylation Changes in Colon Cancer Development – mRNA Expression and Tumor Mutation Alterations
BMC Cancer
Cancer Research
Oncology
Genetics
Amelogenesis Imperfecta and Screening of Mutation in Amelogenin Gene
Case Reports in Dentistry
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Mutation Screening of the Thyroid Peroxidase Gene in a Cohort of 55 Portuguese Patients With Congenital Hypothyroidism
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
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