48th annual meeting and international conference of the Indian Society of Human Genetics 2024: fostering collaborations within rare disease research community
Author:
Funder
Indian National Science Academy
Department of Biotechnology
CSIR
Science and Engineering Research Board
Publisher
Elsevier BV
Reference5 articles.
1. Targeted long-read sequencing identifies missing disease-causing variation;Miller;Am J Hum Genet,2021
2. Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial;Burn;Lancet,2020
3. Cancer prevention with resistant starch in Lynch syndrome patients in the CAPP2-randomized placebo controlled trial: planned 10-year follow-up;Mathers;Cancer Prev Res (Phila),2022
4. A de novo paradigm for male infertility;Oud;Nat Commun,2022
5. National policy for rare diseases 2021;Ministry of Health & Family Welfare,2021
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