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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1989 2
1991 1
1994 2
1995 1
1999 2
2006 1
2010 3
2011 3
2014 1
2016 1
2017 3
2018 1
2019 1
2021 1
2023 1
2024 0

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23 results

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Page 1
Asian paralysis syndrome.
Phadke MA, Gambhir PS, Deshpande AS, Kurlekar SU, Godbole KG. Phadke MA, et al. Among authors: gambhir ps. Ann Trop Paediatr. 1999 Dec;19(4):317-20. doi: 10.1080/02724939992130. Ann Trop Paediatr. 1999. PMID: 10716023
KBG syndrome: 16q24.3 microdeletion in an Indian patient.
Srivastava P, Gambhir PS, Phadke SR. Srivastava P, et al. Among authors: gambhir ps. Clin Dysmorphol. 2017 Jul;26(3):161-166. doi: 10.1097/MCD.0000000000000168. Clin Dysmorphol. 2017. PMID: 28099180 Review. No abstract available.
Pyruvate Carboxylase Deficiency Mimicking Diabetic Ketoacidosis.
Mangla P, Gambhir PS, Sudhanshu S, Srivastava P, Rai A, Bhatia V, Phadke SR. Mangla P, et al. Among authors: gambhir ps. Indian J Pediatr. 2017 Dec;84(12):959-960. doi: 10.1007/s12098-017-2430-1. Epub 2017 Aug 23. Indian J Pediatr. 2017. PMID: 28831725 No abstract available.
Argininemia.
Gambhir PS, Phadke MA, Khedkar VA, Padalkar JA, Joshi AS, Limaye AS, Bhate SM. Gambhir PS, et al. Indian Pediatr. 1989 Dec;26(12):1260-2. Indian Pediatr. 1989. PMID: 2638334 No abstract available.
Trisomy-8.
Phadke MA, Gambhir PS, Pote PD, Padalkar JA, Shirole DB, Joshi AS. Phadke MA, et al. Among authors: gambhir ps. Indian Pediatr. 1986 Mar;23(3):226-7. Indian Pediatr. 1986. PMID: 3744488 No abstract available.
Craniomicromelic syndrome: first report in a male.
Gambhir PS, Gambhir S. Gambhir PS, et al. Am J Med Genet A. 2011 Mar;155A(3):586-8. doi: 10.1002/ajmg.a.33451. Epub 2011 Feb 18. Am J Med Genet A. 2011. PMID: 21337684
23 results