dr. Farmaditya Eka Putra, S.Ked, M.Si.Med, Ph.D
Biography
Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.
Molecular analyses in indonesian individuals with intellectual disability and microcephaly
PAEDIATRICA INDONESIANA 53 (2), 83-8, 2013
Authors: FEP Mundhofir, RN Tunjungputri, WM Nillesen, BWM van Bon, ...
2013
0 cited
NEURONA: MAJALAH KEDOKTERAN NEURO-SAINS PERHIMPUNAN DOKTER SPESIALIS SARAFÂ …, 2013
Authors: TI Winarni, TA Sumekar, M Belladonna, FEP Mundhofir, SMH Faradz
2013
0 cited
[SL: SN], 2013
Authors: FEP Mundhofir
2013
1 cited
Cover prosiding: the fragile x-associated tremor ataxia syndrome (fxtas) in indonesia
JOHN WILEY & SONSLTD, 2013
Authors: TI Winarni, FEP Mundhofir, A Ediati, M Belladonna, WM Nillesen, ...
2013
0 cited
NEURONA (MAJALAH KEDOKTERAN NEURO SAINS PERHIMPUNAN DOKTER SPESIALIS SARAFÂ …
Authors: TA Sumekar, M Belladona, FEP Mundhofir, SMH Faradz
2013
0 cited
GENETIC TESTING AND MOLECULAR BIOMARKERS 16 (3), 162-166, 2012
Authors: TI Winarni, A Utari, FEP Mundhofir, T Tong, B Durbin-Johnson, ...
2012
14 cited
A cytogenetic study in a large population of intellectually disabled indonesians
GENETIC TESTING AND MOLECULAR BIOMARKERS 16 (5), 412-417, 2012
Authors: FEP Mundhofir, TI Winarni, BW Van Bon, S Aminah, WM Nillesen, ...
2012
19 cited
Prevalence of fragile x syndrome in males and females in indonesia
WORLD J MED GENET 2 (3), 2012
Authors: FE Mundhofir, TI Winarni, W Nillesen, BW van Bon, M Schepens, ...
2012
14 cited
Monosomy 9pter and trisomy 9q34. 11qter in two sisters due to a maternal pericentric inversion
GENE 511 (2), 451-454, 2012
Authors: FEP Mundhofir, D Smeets, W Nillesen, TI Winarni, HG Yntema, ...
2012
6 cited
Mowat-wilson syndrome: the first clinical and molecular report of an indonesian patient
CASE REPORTS IN GENETICS 2012, 2012
Authors: FEP Mundhofir, HG Yntema, I van der Burgt, BCJ Hamel, SMH Faradz, ...
2012
4 cited