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Indian Journal of Pediatrics|January 31, 2020
Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian CasesAlec Reginald Errol Correa, Puneeta Mishra, Madhulika Kabra, et al.Journal of Pediatric Genetics|August 14, 2019
Report of a Novel Homozygous Nonsense <i>DDR2</i> Mutation in an Indian Adult Male with Spondylo-meta-epiphyseal Dysplasia, Short Limb-Abnormal Calcification TypeNeerja Gupta, Alec Reginald Errol Correa, Manisha Jana, et al.Annals of Human Genetics|March 3, 2021
Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrumAlec Reginald Errol Correa, Mounika Endrakanti, Kamal Naini, et al.Indian Journal of Pediatrics|May 27, 2020
Methylene Tetrahydrofolate Reductase DeficiencyRavneet Kaur, Alec Reginald Errol Correa, Seema Thakur, et al.Indian Pediatrics|February 16, 2020
Mevalonate Kinase Deficiency as Cause of Periodic Fever in Two SiblingsAlec Reginald Errol Correa, Neerja Gupta, Narendra Bagri, et al.Prenatal Diagnosis|July 24, 2021
Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalisAlec Reginald Errol Correa, Kamal Naini, Pallavi Mishra, et al.American Journal of Medical Genetics. Part A|January 13, 2023
The spectrum of neurological manifestations and genotype-phenotype correlation in Indian children with Gaucher diseaseMahesh Venkatachari, Soumalya Chakraborty, Alec Reginald Errol Correa, et al.Pageof 1