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Decoding the Genetics of Recurrent Molar Pregnancy.
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
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Mutation-Proved Clouston Syndrome in a Large Indian Family with a Variant Phenotype.
Khatter S, Puri RD, Mahay SB, Bhai P, Saxena R, Verma IC.
Khatter S, et al. Among authors: mahay sb.
Indian J Dermatol. 2019 Mar-Apr;64(2):143-145. doi: 10.4103/ijd.IJD_510_17.
Indian J Dermatol. 2019.
PMID: 30983611
Free PMC article.
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Clinico-radiological and biochemical clues to early diagnosis of mucolipidosis type II.
Sandal S, Mahay SB, Gupta D, Saxena R, Verma J, Saxena KK, Puri RD.
Sandal S, et al. Among authors: mahay sb.
Clin Dysmorphol. 2022 Jan 1;31(1):23-27. doi: 10.1097/MCD.0000000000000388.
Clin Dysmorphol. 2022.
PMID: 34561315
No abstract available.
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Prenatal phenotypic spectrum of full trisomy 18 in an Indian cohort.
Sandal S, Mahay SB, Dimri Gupta N, Saxena R, Lall M, Dua Puri R.
Sandal S, et al. Among authors: mahay sb.
Am J Med Genet A. 2022 Jun;188(6):1904-1908. doi: 10.1002/ajmg.a.62692. Epub 2022 Feb 21.
Am J Med Genet A. 2022.
PMID: 35191187
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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
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Case Series of Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase Deficiency.
Narayan V, Mahay SB, Verma IC, Puri RD.
Narayan V, et al. Among authors: mahay sb.
Ann Indian Acad Neurol. 2020 May-Jun;23(3):347-351. doi: 10.4103/aian.AIAN_367_18. Epub 2020 Jun 10.
Ann Indian Acad Neurol. 2020.
PMID: 32606525
Free PMC article.
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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.
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