International Conference

Publication in International Conferences

  1. Faradz SMH, Lego J, Buckley M, Holden JH. Allelic diversity at FMR1, DXS548, and FRAXAC1 in ten Indonesian sub-populations: high prevalence fragile X premutation in an isolated island. Presented in 10th International Workshop of Fragile X and X-linked mental retardation, Frascati, Italia, 19th-20th September 2001.
  2. Faradz SMH, Nillesen W, Sistermans E, Hagerman RJ, Hamel BCJ. A high rate of fragile X in small district of Indonesia can be traced back to one common ancestor. Presented in International Conference on fragile X in Chicago, 17th-20th July 2002.
  3. Faradz SMH, Winarni TI, Setyawati AN, Nielensen W, Mundhofir FEP, Sistermans E, Hamel BCJ. Molecular screening for Fragile X syndrome in institutionalized mild mentally retarded individuals at Temanggung, Central Java (a preliminary study). Presented in 12th International workshop on Fragile X and X-linked mental retardation, Williamsburg (USA), 26th-29th August 2005.
  4. Winarni TI, Setyawati AN, Mundhofir FEP, Faradz SMH, Hamel BCJ, Sistermans E. Excess X chromosome as cause of mental retardation in males. Presented in 17th Asian Conference on Mental Retardation, Yogyakarta. 19th-23rd November 2005.
  5. Siswandari S, Suromo L, Faradz SMH. Diagnostic value of Immunohistochemical test of lymphocytes at peripheral blood smear to detect Fragile X mental retardation syndrome. Presented in 17th Asian Conference on Mental Retardation, Yogyakarta. 19th-23rd November 2005.
  6. Wagenaar JFP, Goris MGA, Adi MS, Hartskeerl RA, van Gorp ECM, Gasem MH. Hemorrhagic complications in severe leptospirosis in Indonesia. Presented in the 4th International Leptospirosis Society Meeting of the society in Chiang Mai, Thailand, 2005.
  7. Mundhofir FEP, Winarni TI, Juniarto AZ, Faradz SMH. Ring Y chromosome in a boy with genital anomaly; a case report. Presented in Pertemuan Ilmiah Nasional, Perhimpunan Ahli Anatomi Indonesia, Semarang 2006
  8. Winarni TI, Mundhofir FEP, Faradz SMH. Identification of Y Chromosome. Presented in Pertemuan Ilmiah Nasional, Perhimpunan Ahli Anatomi Indonesia, Semarang 2006
  9. AB Dessens, Juniarto AZ, Faradz SMH, Drop SLS. Psychosexual development in untreated DSD patients from Indonesia, a pilot study. Presented in 2nd International symposium on disorder of sex development at Luebeck, Germany, 31st August – 2nd September 2006.
  10. Winarni TI, Mundhofir FEP, Faradz SMH. Cytogenetic finding in females with Short Stature. Presented in Pertemuan Ilmiah Nasional, Perhimpunan Ahli Anatomi Indonesia, Padang 2007.
  11. Winarni TI, Mundhofir FEP, Purwanti A, Nillesen W, Sistermans S, Faradz SMH, Hamel BCJ. Profile of mental retardation cases in Semarang Indonesia, 13th International Workshop on Fragile X and X-Linked Mental Retardation, 3-6 October 2007, Lido, Italy.
  12. Winarni TI, Mundhofir FEP, Purwanti A, Kooper A, Nillesen W, Sistermans E, Faradz SMH, Hamel BCJ, Profile of Mental Retardation Cases in Semarang Indonesia. Presented in 13th XLMR Conference , Venice, Italy 2007
  13. Mundhofir FEP, Kooper AJA, Winarni TI , Sistermans E, Smits APT, Faradz SMH, Hamel BCJ. The genetic and clinical impact of a familial marker Der(22)T(8;22). The 7th Human Genome Organization (HUGO)-Pacific Meeting and the 8th Asia-Pacific Conference on Human Genetics 2007-2008.
  14. Faradz SMH, Juniarto AZ, Darmono, Djokomoeljanto R, Drop SLS. Frequency and distribution of patients with ambiguous genitalia in Semarang, Indonesia. Presented at ASEAN Federatin of Endocrine Societies Congress (AFES), Kuala Lumpur, Malaysia, 1st December 2007.
  15. Wagenaar JFP, Goris MGA, Garlanda C, Gasem MH, Haartskeerl RA, van Gorp ECM. Long pentraxin PTX3 predicts mortality in severe leptospirosis. Presented in the 5th International Leptospirosis Society meeting of the society in Quito, Ecuador, 2007.
  16. Ediati A. Dilemmas in communicating with DSD patients and parents. Presented at the 2nd Seminar and Workshop Ambiguous Genitalia and Hypospadia”. Proceeding. Semarang October 17-19, 2008
  17. Mundhofir FEP, Kooper AJA, Winarni TI , Sistermans E, Smits APT, Faradz SMH, Hamel BCJ. The genetic and clinical impact of a familial marker Der(22)t(8;22). Presented in HUGO AP, Philippine, 2008
  18. Winarni TI, Juniarto AZ, Faradz SMH, Hamel BCJ. Chromosomal findings among females with primary amenorrhea. Presented in 7th Human Genome Organization (HUGO)-Pasific Meeting and the 8th Asia-Pacific Conference on Human Genetics on Genomics for Better Health in The Asia Pacific April 2-5, 2008, Cebu, Philippines.
  19. Ediati A, Juniarto AZ, Faradz SMH. biopsychosocial aspect of disorders of sex development (DSD): the role and challenges for psychologist in Indonesia. (in Bahasa Indonesia) Presented at the First National Conference on Biopsychology. Proceeding. Yogyakarta, January 27, 2009
  20. Ediati A, Juniarto AZ, Faradz SMH. Psychosexual impact of late identification on familial congenital adrenal hyperplasia cases. Presented at the First National Conference on Biopsychology. Yogyakarta, January 27, 2009
  21. Maharani N, Setyawati AN, Rifqi S, Sungkar MA, Purwanti A, Faradz SMH, Pals G. Marfan syndrome in Indonesia: report of two cases. Presented in International Seminar and Workshop on Modern Biology and its application Semarang, November 28-30, 2009.
  22. Ediati A, Juniarto AZ, Faradz SMH. Complexities in management of disorders of sex development (DSD): ethical aspect. Presented at the Round Table Discussion on Bioethics in Genetic Disease”. Semarang, February 3, 2009 Winarni TI, Juniarto AZ, Ediati A, Faradz SMH. Disorders of Sex Development in Person with Sex Chromosomal Abnormalities: Learning Disabilities Issues. Presented at the 2nd Asia Pacific Congress of International Association for the Scientific Study of Intellectual Disabilities (IASSID). Singapore, June 24-27, 2009
  23. Mundhofir FEP, Nillesen W, Ruiterkamp-Versteeg M, Schobers G, Winarni TI, Ijntema H, Faradz SMH, Hamel BCJ. Subtelomeric deletion and duplication screening using MLPA analysis in unexplained mental retardation individuals in Semarang Indonesia: A preliminary study. Presented in IASSID 2nd ASIA PACIFIC REGIONAL CONGRESS Singapore 24 June, 2009.
  24. Armalina D, Winarni TI, Mundhofir FEP, Purwanti A, Faradz SMH. Phenotype and cytogenetic profile of Down syndrome cases in special schools in Semarang. Presented in International Seminar and Workshop on Modern Biology and its application Semarang, November 28-30, 2009.
  25. Muniroh M, Jamal RA, Winarni TI, Faradz SMH, Othman Z. Analysis of KRAS2 gene mutations in colorectal cancer patients in Malaysia. Presented in International Seminar and Workshop on Modern Biology and its application Semarang, November 28-30, 2009.
  26. Mundhofir FEP, van Bon BVM, Winarni TI, Nillesen W, Yntema HG, Smeets DFCM, Faradz SMH and Hamel BCJ. A case report of Wolf-Hirschhorn syndrome (WHS): the importance of a MLPA test confirmation. Presented in International Seminar and Workshop on Modern Biology and its application Semarang, November 28-30, 2009.
  27. Ediati A. Psychosocial aspect of genetic diagnostic: experiences from Indonesia. Presented at the International Seminar and Workshop on Modern Biology and its Applications: Focusing on Stem Cell and Human Genetics. Proceeding. Semarang, November 28, 2009.
  28. Ediati A. Psychological aspect of genetic disease and its implication on family-based psychology. (in Bahasa Indonesia) Presented at the National Seminar on Health Psychology: Community empowerment in treating health problem and genetic disease in Indonesia. Proceeding. Semarang, November 30, 2009.
  29. Utari A, Long KP, Tong T, Winarni TI, Mundhofir FEP, SMH Faradz, Tassone F. Blood spots screening for the identification of expanded alleles in the FMR1 gene among intellectual disability students in Indonesia  using  rapid polymerase chain reaction. Presented in International Seminar and Workshop on Modern Biology and its application Semarang, November 28-30, 2009.
  30. Utari A, Chonchaiya W, Rivera SM, Schneider A, Faradz SMH, Hagerman RJ. Time for a controlled trial of minocycline for fragile X syndrome. Presented at the 14th International Workshop on Fragile X and X-Linked Mental Retardation, 2009, Bahia, Brazil.
  31. Chonchaiya W, Utari A, Wang L, Berry-Kravis EM, Hervey C, Au J, Sorensen P, Casillas M, Lohse K, Boyd A, Chambliss B, Cook K, Dandekar R, Gane L, Hagerman RJ. Total clinical ascertainment of daughters who have fathers with fragile X associated tremor ataxia syndrome. Presented at the 14th International Workshop on Fragile X Syndrome and X-linked mental retardation, Bahia, Brazil, September 15-19, 2009.
  32. Tri Indah Winarni, Achmad Zulfa Juniarto, Annastasia Ediati, Sultana MH Faradz. Disorders of sex development in person with sex chromosomal abnormalities: learning disabilities issues. Presented in 2nd IASSID Asia-Pacific Regional Conference, Singapore, June 24-27, 2009.
  33. Clinical involvement in young male individuals with the fragile X premutation. Presented at the 12th International Fragile X Conference, Detroit, Michigan, USA, 21st-25th July 2010.
  34. Winarni TI, Utari A, Mundhofir FEP, Long KP, Tong T, Faradz SMH, Tassone F.Identification of expanded alleles of the FMR1 gene among high risk population in Indonesia using blood spot screening. Presented at the 12th International Fragile X Conference Detroit, Michigan, July 21-25, 2010.
  35. Faradz SMH, Mundhofir FEP, Winarni TI, Nillesen WM, Yntema HG, Hamel BCJ. Genetic counseling difficulties of fragile X cases in Indonesia. Presented on 12th International Fragile- X, Detroit Michigan, USA July 21st – 25th 2010.
  36. Utari A, Adams E, Berry-Kravis E, Chavez A, Scaggs F, Ngotran L, Boyd A, Hessl D, Gane LW, Tassone F, Tartaglia N, Leehey MA, Hagerman RJ. Medical problems associated with aging in individuals with fragile X syndrome. Presented at the 12th International Fragile X Conference, Detroit, Michigan, July 21-25, 2010.
  37. Ediati, A. Mental retardation in children with congenital adrenal hyperplasia. Presented at the Update on Disorder of Sex Development (DSD). Semarang, August 18, 2010
  38. Ediati A, Muniroh M, Setyawati BA, Juniarto AZ, Faradz SMH, de ong FH, Dessens AB, Drop SLS. Physical and psychological dilemma in late identified congenital adrenal hyperplasia (CAH). Presented in the 5th Australian Health and Medical Research Congress (AHMRC) Melbourne, Australia, 14th – 18th November 2010.
  39. Ediati A, Muniroh M, Setyawati BA, Juniarto AZ, Faradz SMH, de Jong FH, Dessens AB, Drop SLS. Physical and psychological dilemma in late identified congenital adrenal hyperplasia (CAH). Poster presentation. Presented at the Human Genetic Society of Australasia (HGSA) conference. Melbourne, November 14-18, 2010
  40. Siemiatkowska AM, Arimadyo K, Moruz LM, de Castro-Miro M, Strom TM, Faradz SMH, Cremers FPM, Hollander AI, Collin RWJ. Molecular genetic analysis of non-syndromic retinitis pigmentosa in Indonesia. Presented in ARVO, Fort Lauderdale, Florida, May 2011.
  41. Faradz SMH, Ediati A, Setyawati BA, Junairto AZ, White S, Bruggenwirth HT, Drop SLS. Genetic counseling in the family with multiple affected of disorder of sex development (DSD): the impact of culture in Indonesia. Poster presentation. Presented at the Human Genetic Society of Australasia (HGSA) conference. Melbourne, November 14-18, 2010.
  42. Mundhofir FEP, Winarni TI, Bon BV, de Leeuw N, Mexitalia E, Yntema HG, Faradz SMH, Hamel BCJ. Multiple congenital anomalies due to a terminal gain of 16P: a case report. Presented in Human Genome Meeting 2011 Dubai, UAE, 14th – 17th, 2011
  43. Ediati A, Juniarto AZ, Drop SLS, Faradz SMH, Dessens AB. Body Image and Sexuality in Indonesian treated and untreated subjects with a disorder of sex development (DSD). Poster presentation. Presented at the 3rd Symposium on Disorder of Sex Development, Lüebeck-Germany, May 19-22, 2011
  44. Ediati A, Juniarto AZ, Drop SLS, Faradz SMH, Dessens AB. Body image and psychosexual functioning in late identified indonesian adults with a disorder of sex development (DSD). Poster presentation. Presented at the 37th Annual International Academy of Sex Research (IASR) conference, UCLA Los Angeles, August 10-13, 2011
  45. Faradz SMH, Mundhofir FEP, Juniarto AZ, Maharani N, Muniroh M, Ediati A, Drop SLS, Hamel BCJ.  Phenotype profiles in congenital adrenal hyperplasia cases with intellectual disabilities. Presented at the 15th International workshop on Fragile X and other early-onset cognitive disorders, Berlin Germany, September 4-7, 2011
  46. Farmaditya EP Mundhofir, Willy M Nillesen, Tri I Winarni, Bregje WM van Bon, Ben CJ Hamel, Helger G Yntema, Sultana MH Faradz. Clinical and molecular studies on fragile X syndrome in Indonesia show equal prevalence in males and females. HUGO meeting, Sydney 11-12 March 2012.
  47. Tri Indah Winarni, Agustini Utari, Farmaditya EP Mundhofir, Tzuhan Tong2, Blythe Durbin-Johnson3, Sultana MH Faradz1, Flora Tassone2,4. A rapid inexpensive FMR1 testing using blood spot for the detection high premutation cases among high-risk population in Indonesia. HUGO meeting, Sydney 11-12 March 2012.
  48. Nani Maharani, Peili Li, Nobuhito Ikeda, Toshihiro Hamada, Kazuhide Ogino, Yasuaki Shirayoshi, Yasutaka Yamamoto, Masanari Kuwabara, Kazuhiro Yamamoto, Ichiro Hisatome. Identification of mRNA expression of urate transporters in mice’s organs Oral Presentation in the 47th Annual Meeting of Japanese Society of Gout and Nucleic Acid Metabolism, Kobe, Japan, February 21st 2014.
  49. Nani Maharani, Peili Li, Masanari Kuwabara, Takeshi Yamashita, Kazuhiro Yamamoto, Yasutaka Kurata, Yasuaki Shirayoshi, Ichiro Hisatome.Uric acid enhanced Kv1.5 channel expression in atrial myocytes via activation of uric acid transporters, xanthine oxidase-dependent oxidative stress and ERK pathway. Oral Presentation in The 78th Annual Scientific Meeting of The Japanese Circulation Society. Tokyo, March 21st 2014.
  50. Utari Agustini, Suhartono, Anwar A, Budiyono. Thyroid Profile of Indonesian Children living in Agricultural Area. Presented at the Australia Paediatric Endocrine Group (APEG) Meeting, Sydney-Australia, 28-31 July, 2013.
  51. Mexitalia M, Utari Agustini, Soetadji A, Subagio HW. Early Risk of Atherosclerosis and Metabolic Syndrome in Nonalcoholic Fatty Liver Indonesian Children. Presented at the International Congress of Pediatrics 2013 (ICP), Melbourne-Australia, August 24-29, 2013.
  52. Soetadji A, Suhartono, Kartini A, Budiyono, Hardaningsih G, Utari A. Elastic artery properties profile of children living in area of chronic organophosphate exposure : a preliminary study. Presented at the International Conference on Tropical and Coastal Region Eco-development 2014, Semarang, 11-13 Agustus 2014.
  53. Tri Indah Winarni, Henna Rya Sunoko, Susilo Wibowo. Insecticides exposure during early life alters prostate cell differentiation in adulthood SD rat. International Conference of Tropical and Coastal Region Eco-development, Semarang, August 11th – 13th, 2014.
  54. Utari Agustini, Ediati A, Ariani MD, Istiadi H, Juniarto AZ, Dessens AB, Drop SLS, Faradz SMH. Challanges in the management of affected children with different gender in multiplex CAH family. Delayed referral : a challanges in the clinical management of CAH in Indonesia. Presented at the 5th International DSD symposium, Ghent, Belgium, 11-13 June 2015.
  55. Ediati A, Utari A, Ariani MD, Istiadi H, Juniarto AZ, Dessens AB, Drop SLS, Faradz SMH. Health-care seeeking behavior in late identified patients with Congenital Adrenal Hyperplasia (CAH) in Central Java, Indonesia. Presented at the 5th International DSD symposium, Ghent, Belgium, 11-13 June 2015.
  56. Faradz SMH, Utari Agustini, Ediati A, Ariani MD, Juniarto AZ. Phenotype variation in untreated 46 XX congenital adrenal hyperplasia. Presented at the 11 th Asia Pasific Conference of Human Genetic 2015, Hanoi-Vietnam. Available at : Ann Transl Med 2015;3(S2):AB079.
  57. Tri Indah Winarni, Costrie Ganes Widayanti, Susilo Wibowo, Randi J. Hagerman, Sultana MH Faradz. The consequences of molecular diagnosis in carriers fragile X syndrome: psychopathological symptoms co-morbidity in Indonesia. 2nd International Conference on FMR1 Premutation: Basic Mechanisms and Clinical Involvement. September 30th – October 2nd 2015, Sitges, Barcelona.
  58. Nani Maharani, Peili Li, Cheng Jidong, Masanari Kuwabara, Kazuhiro Yamamoto, Ichiro Hisatome. Hyperuricemia-induced stabilization of Kv1.5 protein. Oral presentation at The 49th Annual Meeting of The Japanese Society of Gout and Nucleic Acid Metabolism. Osaka, February 18th 2016.
  59. Nani Maharani, Peili Li, Masanari Kuwabara, Junichiro Miake, Takeshi Yamashita, Kazuyoshi Ogura, Kazuhiro Yamamoto, Yasutaka Kurata, Yasuaki Shirayoshi, Ichiro Hisatome. Molecular mechanism underlying urate-induced enhancement of Kv1.5 channel expression in atrial myocytes. Poster presentation at The 79th Annual Scientific Meeting Japanese Circulation Society, Osaka, April 24-26th 2015.
  60. Nani Maharani, Peili Li, Masanari Kuwabara, Takeshi Yamashita, Kazuhiro Yamamoto, Yasutaka Kurata, Yasuaki Shirayoshi, Ichiro Hisatome. The activity of urate to increase Kv1.5 channel expression in atrial myocytes depends on uric acid transporters, xanthine oxidase and ERKs. Oral presentation at 29th Annual Meeting of the Japanese Heart Rhythm Society. Tokyo, Japan, July 23rd-25th 2014.
  61. Suhartono, Subagio HW, Kartini A, Budiyono, Utari Agustini, Suratman. Pesticide exposure and thyroid function among primary school children living in agricultural area. Presented at the Conference of International Society for Environmental Epidemiology and International Society of Exposure Science-Asia Chapter 2016 ( ISEE-ISES AC 2016) , Sapporo, Japan, June 26-29, 2016.
  62. Ediati A &Utari Agustini. Midwives knowledge and attitude towards disorders of sex development (DSD) and its psychological impact. Presented at the 31th International Congress of Psychology, Yokohama-Japan, July 24-29, 2016. Available at: International Journal of Psychology vol 51, Issue supplement S1.p.613.
  63. Nydia Rena Benita Sihombing, Sultana MH Faradz. A patient with multiple congenital anomalies and developmental delay. Presented at Unknown Case Presentation, Asia Pacific Society of Human Genetics (APSHG) Summer School, Hongkong, 26-28 August 2016.
  64. Winarni, T. I., Aziman, M. A., Andar, A. A., & Pawitra, I. The Effect of Early Mosquito Insecticides Exposure on SpraqueDawley Rat Testis: A Histopathological Feature Towards Malignancy? Presented at The 2nd International Conference on Tropical and Coastal Region Eco-Development, Bali, Indonesia, October 25th – 26th, 2016.
  65. Utari Agustini, Ariani MD, Ediati A, Juniarto AZ, Faradz SMH. Mortality Problems of Congenital Adrenal Hyperplasia in Central Java-Indonesia: 12 years experiences. Presented at the 9th biannual meeting of Asia Pacific Pediatric Endocrine Society (APPES) – 50th scientific meeting of Japanese Society for Pediatric Endocrinology (JSPE), Tokyo, 16-20 November 2016.
  66. Utari Agustini, Saldi SRF, Parwoto BTA, Batubara JRL. The effect of glucocorticoid treatment on bone mineral density in children with congenital adrenal hyperplasia: systematic review and meta-analysis. Presented at the 9th biannual meeting of Asia Pacific Pediatric Endocrine Society (APPES) – 50th scientific meeting of Japanese Society for Pediatric Endocrinology (JSPE), Tokyo, 16-20 November 2016. (oral presentation)
  67. Nurin Aisyiyah Listyasari, Achmad Zulfa Juniarto, Sultana MH Faradz. Three cases of 46,XYinconspicuous penis with obesity. Presented at 1st Indonesian Society of Human Genetics (INASHG) Conference and Symposium, Semarang, Indonesia, 26-28 November 2016. (Poster Presentation)
  68. Nydia Rena Benita Sihombing, Shyrien Amalina, Sultana MH Faradz. A female baby with multiple congenital anomalies suspected pfeiffer syndrome. Presented at 1st Indonesian Society of Human Genetics (INASHG) Conference and Symposium, Semarang, Indonesia, 26-28 November 2016. (Poster Presentation)
  69. Nani Maharani, Peili Li, Endang Mahati, Yasuaki Shirayoshi, Kazuhiro Yamamoto, Ichiro Hisatome. Metabolic stress of hyperuricemia stabilizes atrial Kv1.5 channel protein through phosphorylation of heat shock factor 1. Poster presentation at the 81st Annual Meeting of the Japanese Circulation Society. Kanazawa, Japan, March 17-19th 2017.
  70. Nydia Rena Benita Sihombing, Nurin Aisyiyah Listyasari, Sultana MH Faradz. Limb girdle muscular dystrophy in a complex consanguineous family: a clinical follow – up study.Presented at 1st BCM-CUHK Joint Symposium on Clinical Genetics, Hongkong, 20-21 May 2017.(Poster Presentation)
  71. Achmad Zulfa Juniarto, Nurin Aisyiyah Listyasari, Ardy Santosa, Sultana MH Faradz. Microdeletion of azoospermia factor (azf) region in hypospadia patients: a potential factor for infertility. Presented at International Conference on Translational Medicine and Health Sciences. Semarang, Indonesia. 27-28 October 2017.
  72. Nurin Aisyiyah Listyasari, Nydia Rena Benita Sihombing, Tri Indah Winarni. Maria Belladonna. Sultana MH Faradz. Genetic testing and counseling in family with late autosomal dominant spinocerebellar ataxia. Presented at 12th Asia-Pacific Conference on Human Genetics, Bangkok, Thailand, 8-10 November 2017. (Poster Presentation)
  73. Ardy Santosa, Nurin Aisyiyah Listyasari, Achmad Zulfa Juniarto, Sultana MH Faradz. Multidisciplinary management of disorders of sex development in Indonesia: a prototype for developing country. Presented at 19th Annual Congress of Asia Pacific Association of Pediatric Urologists. Yogyakarta, Indonesia. 8-10 November 2017.
  74. Tiar Pratamawati, Nydia Sihombing, Donny Nauphar, Sultana MH Faradz. A family with three children of rare intelectual disability syndrome. Presented at The 12th Asia-Pacific Conference on Human Genetics-APCHG 2017. 8-10 November 2017, Bangkok, Thailand. (Poster Presentation)
  75. Juniarto AZ. Distribution of azoospermia factor (AZF) microdeletions in infertile males admitted to CEBIOR, Semarang, Indonesia. The 12th Asia-Pacific Conference on Human Genetics-APCHG 2017. 8-10 November 2017, Bangkok, Thailand.
  76. Tri Indah Winarni. Aberrant behavior profile of fragile X syndrome in the intellectual disability population with barely gets services. The 12th Asia-Pacific Conference on Human Genetics-APCHG 2017. 8-10 November 2017, Bangkok, Thailand.
  77. Sultana MH Faradz. Genetic diagnosis and experiences in management of disorders of sex development in Indonesia. The 12th Asia-Pacific Conference on Human Genetics-APCHG 2017. 8-10 November 2017, Bangkok, Thailand.
  78.  Nani Maharani, Amallia N Setyawati, Sodiqur Rifqi, MA Sungkar, Gerard Pals, Sultana MH Faradz. Variable major phenotypes in familial Marfan syndrome in Indonesia: a case report. Poster presentation. Presented in 12th Asia-Pacific Conference on Human Genetics-APCHG 2017. 8-10 November 2017, Bangkok, Thailand.