dr. Agustini Utari, S.Ked, Sp.A, M.Si.Med
Biography
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INTERNATIONAL JOURNAL OF OCCUPATIONAL AND ENVIRONMENTAL MEDICINE 9 (WWWÂ …, 2018
Authors: S Suhartono, K Apoina, S Hertanto Wahyu, B Budiyono, U Agustini, ...
2018
19 cited
A rare case of trisomy 18 with split-hand/split-foot malformation (shfm)
JOURNAL OF BIOMEDICINE AND TRANSLATIONAL RESEARCH 4 (2), 41-44, 2018
Authors: NRB Sihombing, A Purwanti, A Utari
2018
0 cited
FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY
Authors: TI Winarni, A Utari, FEP Mundhofir, SMH Faradz
2018
0 cited
Charge syndrome: an indonesian case report (hasil turnitin)
FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY
Authors: JJ Pramudita, A Utari, TI Winarni, SMH Faradz
2018
0 cited
Clinical and molecular analysis of noonan syndrome in indonesia: a case report (hasil turnitin)
FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY
Authors: I Mutmainah, WM Nillesen, FEP Mundhofir, TI Winarni
2018
0 cited
A novel non-invasive short synacthen test validated in a healthy paediatric population
ESPE ABSTRACTS 89, 2018
Authors: C Elder, R Vilela, T Johnson, EH Kemp, B Keevil, J Newell-Price, R Ross, ...
2018
0 cited
STEM CELLS 1, 2
Authors: O Nilsson, JM Wit, M Phillip, S Camper, K Rizzoti, A Bendesky, ...
2018
0 cited
Diagnosis dan tata laksana hiperplasia adrenal kongenital (defisiensi enzim 21-hidroksilase)
BADAN PENERBIT IKATAN DOKTER ANAK INDONESIA, 2018
Authors: A Utari, V Pateda, IM Arimbawa, NP Yati, AB Pulungan, B Tridjaja, ...
2018
0 cited
Charge syndrome: an indonesian case report
JOURNAL OF BIOMEDICINE AND TRANSLATIONAL RESEARCH 3 (1), 23-25, 2017
Authors: JJ Pramudita, A Utari, TI Winarni, SMH Faradz
2017
4 cited