Items where Person is Faradz, Sultana MH

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Armalina, D and Winarni, TI and Mundhofir, Farmaditya EP and Purwanti, A and Faradz, Sultana MH (2009) PHENOTYPE AND CYTOGENETIC PROFILE OF DOWN SYNDROME CASES IN SPECIAL SCHOOLS IN SEMARANG. In: International Seminar and Workshop on Modern Biology and its applications: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang, Indonesia.

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Cahyadi, Misbah Hari and Maharani, Nani and Mundhofir , Farmaditya Eka Putra and Faradz , Sultana MH (2011) UKURAN FISIK ANAK NORMAL USIA 7-12 TAHUN (Studi Pendahuluan pada Siswa SDN Petompon 1 Semarang). Undergraduate thesis, Faculty of Medicine.

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Ediati , Annastasia and Juniarto, Achmad Zulfa and Birnie, Erwin and Okkerse , Jolanda and Croix, Anne de la and Wisniewski, Amy and Drop, Stenvert L.S. and Faradz, Sultana MH (2015) Gender change and stigmatization in late-treated Indonesian children, adolescent, and adult patients with DSD. In: APPES Biennial Scientific 8th, 29 Oktober-1 November 2014, Darwin, Australia.

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Hidayat , Syarif T and Faradz, Sultana MH and Noor-Pramono, NP (2009) CYP19 VNTR POLYMORPHISM A RISK FACTOR IN ENDOMETRIOSIS. In: International Seminar and Workshop on Modern Biology and its applications: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang, Indonesia.

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Mufida, Khilayatul and Juniarto, Zulfa and Faradz , Sultana MH (2015) ANALISIS PREVALENSI DAN FAKTOR RISIKO PASIEN DENGAN ISOLATED HYPOSPADIAS DI LABORATORIUM CEBIOR. Undergraduate thesis, Faculty of Medicine.

Muniroh, Muflihatul and Jamal, Rahman A and Winarni, Tri I and Faradz, Sultana MH and Othman, Zulhabri (2009) Analysis of KRAS2 Gene Mutations in Colorectal Cancer Patients in Malaysia. In: International Seminar and Workshop on Modern Biology and its applications: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang, Indonesia.

Mundhofir, Farmaditya EP and van Bon, Bregje and Winarni, Tri Indah and Nillesen, Willy and Smeets, Dominique and Faradz, Sultana MH and Hamel, Ben CJ (2009) A Case Report of Wolf-Hirschhorn Syndrome (WHS) The Importance of a MLPA test confirmation. In: International Seminar and Workshop on Modern Biology and its applications: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang.

Maharani, N and Setyawati , AN and Rifqi, S and Sungkar, MA and Purwanti, A and Faradz, Sultana MH and Pals, G (2009) Marfan Syndrome in Semarang: report of two cases. In: International Seminar and Workshop on Modern Biology and its applications: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang, Indonesia.

Mirani, Erna and Juniarto, Achmad Zulfa and Winarni , Tri Indah and Faradz , Sultana MH (2009) Sexual Assignment of Children with Ambiguous Genitalia Based on Cytogenetics and SRY Gene Analysis. In: International Seminar and Workshop on Modern Biology and its application: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang, Indonesia.

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Nugroho, Muhammad Agung and Faradz, Sultana MH (2017) PROFIL SITOGENETIKA DAN DISMORFOLOGI PADA PASIEN DENGAN ANOMALI KONGENITAL MULTIPEL. Undergraduate thesis, Faculty of Medicine.

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Putra, Made Saskabawanta Sukmana and Faradz, Sultana MH and Winarni, Tri Indah (2015) ANALISIS KROMOSOM PADA PENDERITA DENGAN ANOMALI KONGENITAL MULTIPEL DI LABORATORIUM CEBIOR. Undergraduate thesis, Faculty of Medicine.

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Ratnaningrum, Safrina D and Mian, Then Sue and Bahtera, Tjipta and Jamal, Rahman A and Faradz, Sultana MH (2009) Screening for HLA-B*1502 Polymorphism in Febrile Seizure Predicted Lead to Epilepsy. In: International Seminar and Workshop on Modern Biology and its applications: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang, Indonesia.

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Sihombing, Kamelia Damaris and Faradz, Sultana MH and Saktini, Fanti (2015) GAMBARAN GEN JAK2 PADA PENDERITA POLISITEMIA VERA DI LABORATORIUM CEBIOR. Undergraduate thesis, Faculty of Medicine.

Saktini, Fanti and Santosa, Santosa and Faradz, Sultana MH Korelasi Mutasi JAK2 V617F dengan Keparahan Klinis pada Pasien Neoplasma Myeloproliferatif yang Memiliki Kromosom Philadelphia Negatif. The 1st Regional Symposium on Health Research And Development .

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Utari, Agustini and Iong, Ka Pou and Tong, Tzuhan and Winarni, Tri Indah and Mundhofir, Farmaditya EP and Faradz, Sultana MH (2009) Blood Spots Screening for the Identification of Expanded Alleles in the FMR1 gene among Intellectual Disability Students in Indonesia using Rapid Polymerase Chain Reaction. In: International Seminar and Workshop on Modern Biology and its applications: Focusing on Stem Cells and Human Genetics, 28-30 November 2009, Semarang, Indonesia.