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Autor:
Ch'ng GS; Department of Genetics, Hospital Pulau Pinang, Ministry of Health, Jalan Residensi, 10990, George Town, Penang, Malaysia., Koh K; Clinical Research Centre, Hospital Kuala Lumpur, Ministry of Health, Jalan Pahang, 50586, Kuala Lumpur, Malaysia. ireth_ere@yahoo.com., Ahmad-Annuar A; Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603, Kuala Lumpur, Malaysia., Taib F; Department of Paediatrics, Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kota Bharu, Kelantan, Malaysia., Koh CL; HELP University, Wisma HELP, Jalan Dungun, Bukit Damansara, 50490, Kuala Lumpur, Malaysia., Lim ESC; Persatuan Kebajikan Ceriajaya Kuala Lumpur Dan Selangor (WeCareJourney), Suite 105, MBE Uptown, No 54, GF, Jalan SS21/58, Damansara Uptown, 47400, Petaling Jaya, Selangor, Malaysia.
Publikováno v:
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 May 16; Vol. 17 (1), pp. 200. Date of Electronic Publication: 2022 May 16.