Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1 by Martínez de LaPiscina, Idoia, Mahmoud, Rana Aa, Sauter, Kay-Sara, Esteva, Isabel, Alonso, Milagros, Costa, Ines, Rial-Rodriguez, Jose Manuel, Rodríguez-Estévez, Amaia, Vela, Amaia, Castano, Luis, Flück, Christa E

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Global, regional, and national burden of spinal cord injury, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 by Safdarian, Mahdi, Trinka, Eugen, Rahimi-Movaghar, Vafa, Thomschewski, Aljoscha, Abady, Gdiom Gebreheat, Abate, Semagn Mekonnen, Abedi, Aidin, Adane, Denberu Eshetie, Afzal, Saira, Ahinkorah, Bright Opoku, Ahmed, Haroon, Angappan, Dhanalakshmi, Aryannejad, Armin, Athari, Seyyed Shamsadin, Atreya, Alok, Babamohamadi, Hassan, Banik, Palash Chandra, Berhie, Alemshet Yirga, Brown, Julie, Champs, Ana Paula, Coberly, Kaleb, Dadras, Omid, Dandona, Rakhi, Dhingra, Sameer, Diao, Nancy, Dibas, Mahmoud, Dongarwar, Deepa, Dsouza, Haneil Larson, Ekholuenetale, Michael, Elhadi, Muhammed, Eskandarieh, Sharareh, Fagbamigbe, Adeniyi Francis, Fatehizadeh, Ali, Fischer, Florian, Ghaffarpasand, Fariborz, Gholamrezanezhad, Ali, Gholizadeh Mesgarha, Milad, Golechha, Mahaveer, Goleij, Pouya, Graham, Simon Matthew, Hamidi, Samer, Harlianto, Netanja I., Hasanian, Mohammad, Hassan, Amr, Hassen, Mohammed Bheser, Iravanpour, Farideh, Irilouzadian, Rana, Jacob, Louis, Jaja, Chinwe Juliana, Joseph, Nitin, Joshua, Charity Ehimwenma, Jozwiak, Jacek Jerzy, Kadashetti, Vidya, Kandel, Amit, Kantar, Rami S., Karaye, Ibraheem M, Karkhah, Samad, Khader, Yousef Saleh, Khan, Ejaz Ahmad, Khan, Md Jobair, Khormali, Moein, Kim, Grace, Kumaran, Senthil D, Mesregah, Mohamed Kamal, Micheletti Gomide Nogueira de Sá, Ana Carolina, Mirza, Moonis, Misganaw, Awoke, Misra, Sanjeev, Mohammadi, Esmaeil, Moni, Mohammad Ali, Mostafavi, Ebrahim, Nassereldine, Hasan, Nguyen, Huong Lan Thi, Nguyen, Van Thanh, Omotayo, Abiodun Olusola, Owolabi, Mayowa O, Patil, Shankargouda, Pawar, Shrikant, Pedersini, Paolo, Pourbagher-Shahri, Ali Mohammad, Rahman, Mosiur, Rahnavard, Niloufar, Rawaf, Salman, Roberts, Nicholas L S, Saeed, Umar, Samadzadeh, Sara, Samy, Abdallah M, Seylani, Allen, Shahbandi, Ataollah, Shetty, Pavanchand H, Yigit, Arzu, Shobeiri, Parnian, Shool, Sina, Sibhat, Migbar Mekonnen, Singh, Paramdeep, Solomon, Yonatan, Umair, Muhammad, Venketasubramanian, Narayanaswamy, Vu, Linh Gia, Yazdanpanah, Fereshteh

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Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases

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