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收藏Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies
Vaseghi, Parisa; Habibi, Laleh; Neidich, Julie A.; Cao, Yang; Fattahi, Neda; Rashidi-Nezhad, Ramin; Salehnezhad, Tayebeh; Dalili, Hossein; Sharbaf, Fatemeh Rahimi; Zarkesh, Mohammad Reza; Malekian, Mahtash; Mokhberdezfuli, Mahdieh; Mehrtash, Amirhosein; Ardeshirdavani, Amin; Kariminejad, Roxana; Ghorbansabagh, Vafa; Sadeghimoghadam, Parvane; Naddaf, Amir; Shirvany, Tahereh Esmaeilnia; Mosayebi, Ziba; Sahebdel, Behrokh; Golshahi, Fatemeh; Shirazi, Mahboobeh; Shamel, Shirin; Moeini, Roksana; Heidari, Abolfazl; Daneshmand, Mohammad Ali; Ghasemi, Reza; Akrami, Seyed Mohammad; Rashidi-Nezhad, Ali 分享 收藏 Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran使用TREC/KREC测定对伊朗严重T和b细胞淋巴细胞减少的新生儿进行筛查Nourizadeh, Maryam; Shakerian, Leila; Borte, Stephan; Fazlollahi, Mohammadreza; Badalzadeh, Mohsen; Houshmand, Massoud; Alizadeh, Zahra; Dalili, Hossein; Rashidi-Nezhad, Ali; Kazemnejad, Anoshirvan; Moin, Mostafa; Hammarstrom, Lennart; Pourpak, Zahra 分享 收藏 
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