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TRI INDAH WINARNI

Professor

Doctoral Program of Medical Science and Health

Medical Faculty


Publications

Prof. Dr. dr Tri Indah Winarni, M.Si.Med

Biography

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Prevalence of fragile x syndrome in males and females in indonesia (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY

Authors: FEP Mundhofir, TI Winarni, WM Nillesen, SMH Faradz

2018

0 cited

Monosomy 9pter and trisomy 9q34. 11qter in two sisters due to a maternal pericentric inversion (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY

Authors: FEP Mundhofir, D Smeets, TI Winarni, SMH Faradz

2018

0 cited

The fragile x-associated tremor ataxia syndrome (fxtas) in indonesia (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY, 2018

Authors: TI Winarni, FEP Mundhofir, A Ediati, M Belladona, SMH Faradz

2018

0 cited

The role of shox gene in short sature of turner syndrome and its variants (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY

Authors: TI Winarni, FEP Mundhofir, SMH Faradz

2018

0 cited

Cytogenetic analysis and clinical phenotype of primary amenorrhea in indonesian patients (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY, 2018

Authors: A Ali, R Indriyati, TI Winarni, SMH Faradz

2018

0 cited

A cytogenetic study in a large population of intellectually disabled indonesians (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY

Authors: FEP Mundhofir, TI Winarni, SMH Faradz

2018

0 cited

Autism phenotype in fragile x premutation males is not associated with fmr1 expression: a preliminary evaluation (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY

Authors: TA Sumekar, TI Winarni, SMH Faradz

2018

0 cited

A small (ssmc) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY

Authors: FEP Mundhofir, TI Winarni, SMH Faradz

2018

0 cited

A cohort study of intellectual disability focusing on fragile x syndrome in indonesia (hasil turnitin)

FACULTY OF MEDICINE, DIPONEGORO UNIVERSITY

Authors: TI Winarni, FEP Mundhofir, SMH Faradz

2018

0 cited

A single common assay for robust and rapid fragile x mental retardation syndrome screening from dried blood spots

FRONTIERS IN GENETICS 9, 582, 2018

Authors: VJ Tan, M Lian, SMH Faradz, TI Winarni, SS Chong

2018

4 cited