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Meckel syndrome: Clinical and mutation profile in six fetuses.
Radhakrishnan P, Nayak SS, Shukla A, Lindstrand A, Girisha KM. Radhakrishnan P, et al. Among authors: nayak ss. Clin Genet. 2019 Dec;96(6):560-565. doi: 10.1111/cge.13623. Epub 2019 Aug 21. Clin Genet. 2019. PMID: 31411728
Symmetrical terminal transverse limb deficiencies.
Agarwal D, Nayak SS, Adiga PK, Phadke SR, Girisha KM. Agarwal D, et al. Among authors: nayak ss. Indian J Pediatr. 2015 May;82(5):478-9. doi: 10.1007/s12098-014-1569-2. Epub 2014 Nov 5. Indian J Pediatr. 2015. PMID: 25366287 No abstract available.
What does fetal autopsy unmask in oligohydramnios?
Nayak SS, Shukla A, Kodandapani S, Adiga PK, Girisha KM. Nayak SS, et al. J Matern Fetal Neonatal Med. 2016;29(14):2347-51. doi: 10.3109/14767058.2015.1085021. Epub 2015 Sep 18. J Matern Fetal Neonatal Med. 2016. PMID: 26381033 Free article.
162 results