نتائج البحث - Sihombing, Nydia
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Clinical manifestation and genetic analysis of familial rare disease genodermatosis xeroderma pigmentosum حسب Yuniati, Renni, Sihombing, Nydia Rena Benita, Nauphar, Donny, Tiawarman, Budi, Kartikasari, Diah Shinta, Dewi, Meira, Faradz, Sultana MH
منشور في 2021نص -
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Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled i... حسب Sihombing, Nydia Rena Benita, Cai, Shiwei, Wong, Daphne Pei Wen, Guan, Ming, Chong, Samuel Siong-Chuan, Faradz, Sultana Muhammad Hussein, Winarni, Tri Indah
منشور في 2021نص -
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Turner syndrome in Diverse Populations حسب Kruszka, Paul, Addissie, Yonit A., Tekendo-Ngongang, Cedrik, Jones, Kelly L., Savage, Sarah K., Gupta, Neerja, Sirisena, Nirmala D., Cerda, Teresa E. Aravena, Nampoothiri, Sheela, Girisha, Katta M., Patil, Siddaramappa Jagdish, Jamuar, Saumya Shekhar, Utari, Agustini, Sihombing, Nydia, Mishra, Rupesh, Chitrakar, Neer Shoba, Iriele, Brenda, Lulseged, Ezana, Megarbane, Andre, Uwineza, Annette, Roque, Milagros M. Duenas, Thong, Meow-Keong, Moresco, Angélica, Obregon, María Gabriela, Ling, Tung Yuet, Mok, Gary TK, Fleischer, Nicole, Rwegerera, Godfrey, de Herreros, María Beatriz, Watts, Jonathan, Fieggen, Karen, Farouk, Dalia, Ashaat, Neveen A., Chung, Brian H.Y., Badoe, Eden, Faradz, Sultana MH, El-Ruby, Mona, Shotelersuk, Vorasuk, Wonkam, Ambroise, Ekure, Ekanem Nsikak, Richieri-Costa, Antonio, Muenke, Maximilian
منشور في 2019نص