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Decoding the Genetics of Recurrent Molar Pregnancy.
Mehta S, Mahay SB, Satapathy A, Arora K. Mehta S, et al. Among authors: mahay sb. J Hum Reprod Sci. 2024 Jan-Mar;17(1):61-64. doi: 10.4103/jhrs.jhrs_121_23. Epub 2024 Mar 28. J Hum Reprod Sci. 2024. PMID: 38665615 Free PMC article.
Next-Generation Sequencing in Unexplained Intellectual Disability.
Sandal S, Verma IC, Mahay SB, Dubey S, Sabharwal RK, Kulshrestha S, Saxena R, Suman P, Kumar P, Puri RD. Sandal S, et al. Among authors: mahay sb. Indian J Pediatr. 2023 Oct 7. doi: 10.1007/s12098-023-04820-5. Online ahead of print. Indian J Pediatr. 2023. PMID: 37804371
Antenatal Phenotype of Desbuquois Dysplasia.
Biji IK, Mahay SB, Saxena R, Verma I, Kumar B, Puri RD. Biji IK, et al. Among authors: mahay sb. Indian J Pediatr. 2023 Jan;90(1):83-86. doi: 10.1007/s12098-022-04386-8. Epub 2022 Nov 4. Indian J Pediatr. 2023. PMID: 36331722
Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India.
Sachdeva A, Jain P, Gunasekaran V, Mahay SB, Mukherjee S, Hagerman R, Shankar S, Kapoor S, Kedia SN; Indian Academy of Pediatrics Consensus in Diagnosis and Management of Fragile X Syndrome Committee.; Indian Academy of Pediatrics Consensus in Diagnosis and Management of Fragile X Syndrome Committee. Sachdeva A, et al. Among authors: mahay sb. Indian Pediatr. 2019 Mar 15;56(3):221-228. Indian Pediatr. 2019. PMID: 30954995 Free article.