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Page 1
Turner syndrome in diverse populations.
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong MK, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, de Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Kruszka P, et al. Among authors: yesodharan d. Am J Med Genet A. 2020 Feb;182(2):303-313. doi: 10.1002/ajmg.a.61461. Epub 2019 Dec 19. Am J Med Genet A. 2020. PMID: 31854143 Free PMC article.
Sirenomelia: case reports and current concepts of pathogenesis.
Pillay M, Yesodharan D, Narayanan DL, Jojo A, Luiz N, Nampoothiri S. Pillay M, et al. Among authors: yesodharan d. Pediatr Dev Pathol. 2012 Sep-Oct;15(5):403-6. doi: 10.2350/12-05-1199-CC.1. Epub 2012 Jul 20. Pediatr Dev Pathol. 2012. PMID: 22816558
Eight years experience from a skeletal dysplasia referral center in a tertiary hospital in Southern India: a model for the diagnosis and treatment of rare diseases in a developing country.
Nampoothiri S, Yesodharan D, Sainulabdin G, Narayanan D, Padmanabhan L, Girisha KM, Cathey SS, De Paepe A, Malfait F, Syx D, Hennekam RC, Bonafe L, Unger S, Superti-Furga A. Nampoothiri S, et al. Among authors: yesodharan d. Am J Med Genet A. 2014 Sep;164A(9):2317-23. doi: 10.1002/ajmg.a.36668. Epub 2014 Jul 14. Am J Med Genet A. 2014. PMID: 25044831
Prenatal diagnosis of nail patella syndrome: A case report.
Padmanabhan LD, Yesodharan D, Nampoothiri S. Padmanabhan LD, et al. Among authors: yesodharan d. Indian J Radiol Imaging. 2017 Jul-Sep;27(3):329-331. doi: 10.4103/ijri.IJRI_438_16. Indian J Radiol Imaging. 2017. PMID: 29089684 Free PMC article.
Plexiform Neurofibroma of Clitoris.
Yesodharan D, Sudarsanan B, Jojo A, Abraham M, Bhavani N, Mathews H, Nampoothiri S. Yesodharan D, et al. J Pediatr Genet. 2017 Dec;6(4):244-246. doi: 10.1055/s-0037-1602789. Epub 2017 May 2. J Pediatr Genet. 2017. PMID: 29142769 Free PMC article.
Osteoglophonic Dysplasia: Phenotypic and Radiological Clues.
Kuthiroly S, Yesodharan D, Ghosh A, White KE, Nampoothiri S. Kuthiroly S, et al. Among authors: yesodharan d. J Pediatr Genet. 2017 Dec;6(4):247-251. doi: 10.1055/s-0037-1602816. Epub 2017 May 5. J Pediatr Genet. 2017. PMID: 29147600 Free PMC article.
Elsahy-Waters syndrome is caused by biallelic mutations in CDH11.
Harms FL, Nampoothiri S, Anazi S, Yesodharan D, Alawi M, Kutsche K, Alkuraya FS. Harms FL, et al. Among authors: yesodharan d. Am J Med Genet A. 2018 Feb;176(2):477-482. doi: 10.1002/ajmg.a.38568. Epub 2017 Dec 22. Am J Med Genet A. 2018. PMID: 29271567
29 results