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

Year Number of Results
1999 1
2000 1
2001 1
2005 1
2006 1
2009 2
2010 5
2011 10
2012 12
2013 9
2014 5
2015 10
2016 3
2017 3
2018 4
2019 10
2020 4
2021 5
2022 8
2023 5
2024 0

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83 results

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Page 1
Training in clinical genetics and genetic counseling in Asia.
Cutiongco-de la Paz EM, Chung BH, Faradz SMH, Thong MK, David-Padilla C, Lai PS, Lin SP, Chen YH, Sura T, Laurino M. Cutiongco-de la Paz EM, et al. Among authors: faradz smh. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):177-186. doi: 10.1002/ajmg.c.31703. Epub 2019 Apr 29. Am J Med Genet C Semin Med Genet. 2019. PMID: 31037827 Review.
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: faradz smh. 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.
Surveillance and prevalence of fragile X syndrome in Indonesia.
Sihombing NRB, Winarni TI, Utari A, van Bokhoven H, Hagerman RJ, Faradz SM. Sihombing NRB, et al. Among authors: faradz sm. Intractable Rare Dis Res. 2021 Feb;10(1):11-16. doi: 10.5582/irdr.2020.03101. Intractable Rare Dis Res. 2021. PMID: 33614370 Free PMC article. Review.
Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes.
Tucker EJ, Bell KM, Robevska G, van den Bergen J, Ayers KL, Listyasari N, Faradz SM, Dulon J, Bakhshalizadeh S, Sreenivasan R, Nouyou B, Carre W, Akloul L, Duros S, Domin-Bernhard M, Belaud-Rotureau MA, Touraine P, Jaillard S, Sinclair AH. Tucker EJ, et al. Among authors: faradz sm. Eur J Hum Genet. 2022 Feb;30(2):219-228. doi: 10.1038/s41431-021-00977-9. Epub 2021 Oct 28. Eur J Hum Genet. 2022. PMID: 34707299 Free PMC article.
Tumor risk in disorders of sex development.
Pleskacova J, Hersmus R, Oosterhuis JW, Setyawati BA, Faradz SM, Cools M, Wolffenbuttel KP, Lebl J, Drop SL, Looijenga LH. Pleskacova J, et al. Among authors: faradz sm. Sex Dev. 2010 Sep;4(4-5):259-69. doi: 10.1159/000314536. Epub 2010 Jun 17. Sex Dev. 2010. PMID: 20558977 Review.
Epidermolysis Bullosa and Rickets in a 21-Year-Old Female: A Case Report.
Yuniati R, Hellmi RY, Dwijayanti GC, Astuti MDK, Pals G, Micha D, Faradz SM. Yuniati R, et al. Among authors: faradz sm. Case Rep Dermatol. 2022 Oct 6;14(3):291-301. doi: 10.1159/000525068. eCollection 2022 Sep-Dec. Case Rep Dermatol. 2022. PMID: 36824157 Free PMC article.
83 results