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Publications by Menitha Poranki
TASP1 Mutation in a Female With Craniofacial Anomalies, Anterior Segment Dysgenesis, Congenital Immunodeficiency and Macrocytic Anemia
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Related publications
Mutation Analysis of the Genes Associated With Anterior Segment Dysgenesis, Microcornea and Microphthalmia in 257 Patients With Glaucoma
International Journal of Molecular Medicine
Medicine
Genetics
Molecular and Developmental Mechanisms of Anterior Segment Dysgenesis
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Novel Mutations in PXDN Cause Microphthalmia and Anterior Segment Dysgenesis
European Journal of Human Genetics
Genetics
Congenital Sideroblastic Anemia in a Female
American Journal of Hematology
Hematology
Psychological Impact of Visible Differences in Patients With Congenital Craniofacial Anomalies
Progress in Orthodontics
A Study of Craniofacial Congenital Anomalies in the Malwa Region (Madhya Pradesh)
Journal of Evolution of Medical and Dental Sciences
Craniofacial Anomalies
International Journal of Pediatric Otorhinolaryngology
Medicine
Otorhinolaryngology
Pediatrics
Perinatology
Child Health
Mutations of a Human Homologue of the Drosophila Eyes Absent Gene (EYA1) Detected in Patients With Congenital Cataracts and Ocular Anterior Segment Anomalies
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Foxf2: A Novel Locus for Anterior Segment Dysgenesis Adjacent to the Foxc1 Gene
PLoS ONE
Multidisciplinary
