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Counselling of patients with inherited or familial disorders for specialties like Obs-Gyne, Paediatrics, Neonatology, Dermatology, Ophthalmology, ENT, Oncology, Orthopedics, etc.
Planning the correct genetic test, ranging from Karyotype to a Whole-Genome sequencing.
Variant analysis and Interpretation of reports which help in Post-test counselling and estimating the recurrence risk of the disorder.
Planning and interpretation of tests for Metabolic disorders seen in patients (neonates/ Paediatrics) with Inborn errors of Metabolism.
The Foundation lays significantemphasis on leveraging technology for developmental solutions.
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