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Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.
Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, Datar C, Verma IC, Puri RD, Zollino M, Bachmann-Gagescu R, Niedrist D, Papik M, Figueiro-Silva J, Masood R, Zweier M, Kraemer D, Lincoln S, Rodan L; Undiagnosed Diseases Network (UDN); Passemard S, Drunat S, Verloes A, Horn AHC, Sticht H, Steinfeld R, Plecko B, Latal B, Jenni O, Asadollahi R, Rauch A. Boonsawat P, et al. Among authors: verma ic. Genet Med. 2019 Sep;21(9):2043-2058. doi: 10.1038/s41436-019-0464-7. Epub 2019 Mar 7. Genet Med. 2019. PMID: 30842647 Free PMC article.
Dysmorphology diagnosis.
Puri RD, Verma IC. Puri RD, et al. Among authors: verma ic. Indian J Pediatr. 2004 Jun;71(6):535-9. doi: 10.1007/BF02724297. Indian J Pediatr. 2004. PMID: 15226565
Spectrum of severe skeletal dysplasias in North India.
Puri RD, Thakur S, Verma IC. Puri RD, et al. Among authors: verma ic. Indian J Pediatr. 2007 Nov;74(11):995-1002. doi: 10.1007/s12098-007-0183-y. Indian J Pediatr. 2007. PMID: 18057679
Molecular studies of achondroplasia.
Nahar R, Saxena R, Kohli S, Puri R, Verma IC. Nahar R, et al. Among authors: verma ic. Indian J Orthop. 2009 Apr;43(2):194-6. doi: 10.4103/0019-5413.50856. Indian J Orthop. 2009. PMID: 19838370 Free PMC article.
413 results