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Expanding the phenome and variome of skeletal dysplasia.
Maddirevula S, Alsahli S, Alhabeeb L, Patel N, Alzahrani F, Shamseldin HE, Anazi S, Ewida N, Alsaif HS, Mohamed JY, Alazami AM, Ibrahim N, Abdulwahab F, Hashem M, Abouelhoda M, Monies D, Al Tassan N, Alshammari M, Alsagheir A, Seidahmed MZ, Sogati S, Aglan MS, Hamad MH, Salih MA, Hamed AA, Alhashmi N, Nabil A, Alfadli F, Abdel-Salam GMH, Alkuraya H, Peitee WO, Keng WT, Qasem A, Mushiba AM, Zaki MS, Fassad MR, Alfadhel M, Alexander S, Sabr Y, Temtamy S, Ekbote AV, Ismail S, Hosny GA, Otaify GA, Amr K, Al Tala S, Khan AO, Rizk T, Alaqeel A, Alsiddiky A, Singh A, Kapoor S, Alhashem A, Faqeih E, Shaheen R, Alkuraya FS. Maddirevula S, et al. Among authors: kapoor s. Genet Med. 2018 Dec;20(12):1609-1616. doi: 10.1038/gim.2018.50. Epub 2018 Apr 5. Genet Med. 2018. PMID: 29620724 Free article.
Short syndrome-an expanding phenotype.
Singh A, Arora R, Singh P, Kapoor S. Singh A, et al. Among authors: kapoor s. Indian Pediatr. 2013 Apr;50(4):414-6. doi: 10.1007/s13312-013-0099-8. Indian Pediatr. 2013. PMID: 23665600 Free article.
Genetic study of an Indian family with cherubism.
Singh A, Singh K, Goel R, Hu Y, Reichenberger E, Kapoor S. Singh A, et al. Among authors: kapoor s. Indian J Pediatr. 2014 Mar;81(3):299-301. doi: 10.1007/s12098-013-1195-4. Epub 2013 Sep 5. Indian J Pediatr. 2014. PMID: 24005878
2,104 results