Items where Subject is "Q Science > QH Natural history > QH426 Genetics"

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Number of items at this level: 65.

A

Achmadi, Joelal (2008) Nutrisi Dan Reproduksi. Badan Penerbit Universitas Diponegoro, Semarang. ISBN 978-979-704-590-6

Ali, Aisha and Indriyati, Rita and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) Cytogenetic Analysis and Clinical Phenotype of Primary Amenorrhea in Indonesian Patients (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

B

Berlinda, Impi and Faradz, Sultana M H and Eka Putra, Farmaditya (2015) Distribusi Penderita Sindrom Down Berdasarkan Analisis Sitogenetika Di Laboratorium CEBIOR. Undergraduate thesis, Faculty of Medicine.

E

Elfitasari, Tita (1999) Study of Population Genetics As a Tool for Determining Larval Dispersal and Recruitment of Marine Species. Documentation. FAKULTAS PERIKANAN DAN ILMU KELAUTAN.

F

Faradz, Sultana M.H. (2005) The Genetic Of Mental Retardation. In: 17th ACMR Conference, 18 - 23 Nov 2005, Yogyakarta.

Faradz, Sultana M.H. and Pattiiha, M Z and Leigh, D A and Jenkins , M and Leggo, J and Buckley, Michael F and Holden, J J A (2000) Genetic diversity at the FMR1 locus in the Indonesian population. Annals of Human Genetics , 64 (04). pp. 329-333.

H

Hermawati, Donna and Then, Sue-Mian and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) Lower Erythrocyte GST Activity in Autism Spectrum Disorder (ASD) Patients Compared to Normal Controls (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

I

Ira, Pirsa Hatpri Nur and Faradz, Sultana M.H. and Ariani, Mahayu Dewi (2015) ANALISIS SITOGENETIKA PADA PASIEN DENGAN AMENORE PRIMER DI CENTER FOR BIOMEDICAL RESEARCH (CEBIOR) SEMARANG. Undergraduate thesis, Faculty of Medicine.

K

Kusumaningrum, Hermin Pancasakti Polder Tawang Semarang : Study Case of Biotechnological Application and Waste Water treatment as part of Integrated Coastal Management. In: UNSPECIFIED.

Kusumaningrum, Hermin Pancasakti (2010) SYLLABUS OF GENETIC ENGINEERING COURSES ON BIOLOGY STUDY PROGRAM. [Teaching Resource] (Unpublished)

Kusumaningrum, Hermin Pancasakti SYLLABUS OF MICROBIAL GENETIC COURSES ON BIOLOGY STUDY PROGRAM. [Teaching Resource] (Unpublished)

Kusumaningrum, Hermin Pancasakti (2008) Characterization of Green Algae Dunaliella sp and Cyanobacterial Isolate and Detection of the DXS Gene Encoding the Key Enzyme in Carotenoid Biosynthesis. PhD thesis, Universitas Diponegoro.

Kusumaningrum, Hermin Pancasakti (2009) INTRASPECIES PROTOPLAST FUSION PROCESS OF Dunaliella salina. In: Recent Advances of 10th Congress and International Conference of Indonesian Society for icrobiology : Microbiology in Health, Bio-Industry, Agriculture and Environment, 20-21 November 2009, Surabaya.

Kusumaningrum, Hermin Pancasakti (2008) MICROBIOLOGICAL AND ECOPHYSIOLOGICAL CHARACTERIZATION OF GREEN ALGAE Dunaliella sp. FOR IMPROVEMENT OF CAROTENOID PRODUCTION. Natur Indonesia , 10 (2). pp. 66-69. ISSN 1410 – 9379

Kusumaningrum, Hermin Pancasakti (2008) MOLECULAR DETERMINATION OF A GREEN ALGAE ISOLATE TO DETECTING 1-Deoxy-D-Xylulose-5-phosphate Synthase (DXS) GENE IN IMPROVEMENT OF CAROTENOID PRODUCTION. Ilmu Kelautan , 11 (2). pp. 79-86. ISSN 0853 – 7291

Kusumaningrum, Hermin Pancasakti (2008) Quantitative production of carotenoid and plasmid stability of Escherichia coli JM 109 pCAR25 Recombinant. Undergraduate thesis, Diponegoro University.

Kusumaningrum, Hermin Pancasakti (2006) SPECIES DETERMINATION OF GREEN ALGAE ISOLATED FROM JEPARA, INDONESIAN COASTAL REGION BASED ON MICROBIOLOGYCAL, ECOPHYSIOLOGICAL AND MOLECULAR CHARACTERIZATION FOR IMPROVEMENT OF CAROTENOID PRODUCTION. Coastal Development , 10 (1). pp. 33-46. ISSN 1410-5271

Kusumaningrum, Hermin Pancasakti SYLLABUS OF MOLECULAR BIOLOGY COURSES ON BIOLOGY STUDY PROGRAM. [Teaching Resource] (Unpublished)

L

Laksono, Bremmy and Maskoen, Ani Melani and Winarni, Tri Indah and Taufik, Syarief and Faradz, Sultana M.H. (2018) Frequency of MTHFR GENE C677T polymorphism for nonsyndromic autism spectrum disorder patients (HASIL TURNITIN). Faculty of Medicine, Diponegoro University. (Unpublished)

Leight, Mary Jacena S. and Nguyen, Danh V. and Winarni, Tri Indah and Schneider, Andrea (2018) A randomized double-blind, placebo-controlled trial of minocycline in children and adolescents with fragile x syndrome (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Lim, Grace X.Y. and Yeo, Minli and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 gene (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Litani, Liem Syeren and Winarni, Tri Indah (2018) HUBUNGAN CAREGIVER BURDEN DENGAN QUALITY OF LIFE (QOL) ORANGTUA DENGAN ANAK AUTISME DAN ORANGTUA DENGAN ANAK DISABILITAS INTELEKTUAL. Undergraduate thesis, Faculty of Medicine.

Liu, Ying and Winarni, Tri Indah (2018) FXTAS in Gey Zone Carriers (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

M

Mundhofir, Farmaditya EP and A.J.A. Kooper, A.J.A. Kooper and Winarni, Tri Indah and A.P.T. Smith, A.P.T. Smith and Faradz, Sultana M.H. and B.C.J. Hamel, B.C.J. Hamel (2010) A SMALL (sSMC) CHROMOSOME 22 DUE TO A MATERNAL TRANSLOCATION BETWEEN CHROMOSOMES 8 AND 22: A CASE REPORT. Journal of Genetic Counseling, 21 (1). pp. 99-108. ISSN 1059-7700

Mundhofir, Farmaditya EP and Nillesen, Willy M. and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) Subtelomeric chromosomal rearrangements in a large cohort of unexplained intellectually disabled individuals in Indonesia: A clinical and molecular study (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Mundhofir, Farmaditya EP and Smeets, Dominique and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversion (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Mundhofir, Farmaditya EP and Tunjungputri, Rahajeng Nareswari and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) Molecular analyses in Indonesian individuals with intellectual disability and microcephaly (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Mundhofir, Farmaditya EP and Winarni, Tri Indah and Estiningtyas, Mexitalia S and Faradz, Sultana M.H. (2018) Multiple Congenital Anomalies Due To a Terminal Gain of 16p; a Case Report (POSTER). Faculty of Medicine, Diponegoro University.

Mundhofir, Farmaditya EP and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) A Cytogenetic Study in a Large Population of Intellectually Disabled Indonesians (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Mundhofir, Farmaditya EP and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) THE GENETIC AND CLINICAL IMPACT OF A FAMILIAL MARKER Der(22)t(8;22) (POSTER). Faculty of Medicine, Diponegoro University.

Mundhofir, Farmaditya EP and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) 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.

Mundhofir, Farmaditya EP and Winarni, Tri Indah and Nillesen, Willy M. and Faradz, Sultana M.H. (2018) Prevalence of fragile X syndrome in males and females in Indonesia (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Mutmainah, Iffa and Nillesen, Willy M. and Mundhofir, Farmaditya EP and Winarni, Tri Indah (2018) Clinical and molecular analysis of Noonan syndrome in Indonesia: a case report (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

N

Ngestiningsih, Dwi and Prasetyo, Antonius Eko and Faradz, Sultana M.H. and Juniarto, Achmad Zulfa (2004) Penampilan Fragile site dalam dua media kultur yang berbeda. Jurnal Kedokteran Yarsi, 12 (3). pp. 25-32.

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

P

Pramudita, Jessica Juan and Utari, Agustini and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) CHARGE Syndrome: An Indonesian Case Report (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

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.

Putri, Pingkan Permata and Dewi, Puspita Kusuma (2017) FAKTOR-FAKTOR YANG MEMPENGARUHI TINGKAT PENGETAHUAN ORANG TUA MENGENAI KELAINAN GENETIK PENYEBAB DISABILITAS INTELEKTUAL DI KABUPATEN KENDAL. Undergraduate thesis, Faculty of Medicine.

S

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 .

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.

Sumekar, Tanjung Ayu and Ashrani , Aneel A. and Winarni, Tri Indah and Hagerman, Randi J. (2018) Monoclonal Gammopathy of Undetermined Significance(MGUS) in a Man with Fragile Xassociated Tremor/Ataxia Syndrome (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

Sumekar, Tanjung Ayu and Winarni, Tri Indah and Faradz, Sultana M.H. (2018) Autism phenotype in fragile X premutation males is not associated with FMR1 expression: a preliminary evaluation (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

T

Tan, Vivienne J. and Lian, Mulias and Faradz, Sultana M.H. and Winarni, Tri Indah (2018) A Single Common Assay for Robust and Rapid Fragile X Mental Retardation Syndrome Screening From Dried Blood Spots (HASIL TURNITIN). Faculty of Medicine, Diponegoro University.

W

Winarni, Tri Indah Association of PDGFRA gene polymorphisms and early-onset myopia in South Sumatera, Indonesia. Asian Journal of Ophthalmology.

Winarni, Tri Indah Attitudes Towards Sexuality in Males and Females with Intellectual Disabilities: Indonesia Setting. Journal of Intellectual Disability - Diagnosis and Treatment.

Winarni, Tri Indah Correlation between Digit Ratio and Incidence of Meningioma and its Clinical Profiles. -.

Winarni, Tri Indah Correlation between Digit Ratio and Incidence of Meningioma and its Clinical Profiles (turnitin). -. (Unpublished)

Winarni, Tri Indah Correlation between Digit Ratio and Incidence ofMeningioma and its Clinical Profiles (Peer Review). -. (Unpublished)

Winarni, Tri Indah A Cytogenetic Study in a Large Population of Intellectually Disabled Indonesians. GENETIC TESTING AND MOLECULAR BIOMARKERS.

Winarni, Tri Indah Early Intervention Combined with Targeted Treatment Promotes Cognitive and Behavioral Improvements in Young Children with Fragile X Syndrome. Hindawi Publisher.

Winarni, Tri Indah Factors Affecting Parents' Acceptance towards Children with Familial Intellectual Disabilities (peer review). -. (Unpublished)

Winarni, Tri Indah Factors Affecting Parents' Acceptance towards Children with Familial Intellectual Disabilities (turnitin). -.

Winarni, Tri Indah Factors Affecting Parents' Acceptance towards Children with Familial Intellectual Disabilities (turnitin). -.

Winarni, Tri Indah Fragile X syndrome: clinical, cytogenetic and molecular screening among autism spectrum disorder children in Indonesia. Clinical Genetics.

Winarni, Tri Indah The fragile X-associated tremor ataxia in Indonesia. Clinical Genetics.

Winarni, Tri Indah (2012) Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriers. Clinical Genetics.

Winarni, Tri Indah Genetic Counseling to Reduce the Level of Depression in Parents of Children with Thalassemia Major (turnitin). -.

Winarni, Tri Indah Immune-Mediated Disorders Among Women Carriers of Fragile X Premutation Alleles. American Journal of Medical Genetics.

Winarni, Tri Indah Monoclonal Gammopathy of Undetermined Significance (MGUS) in a Man with Fragile X-associated Tremor/Ataxia Syndrome. Hindawi Publisher.

Winarni, Tri Indah A Randomized Double-Blind, Placebo-Controlled Trial of Minocycline in Children and Adolescents with Fragile X Syndrome. Wolters Kluwer.

Winarni, Tri Indah Sertraline May Improve Language Developmental Trajectory in Young Children with Fragile X Syndrome: A Retrospective Chart Review. Hindawi Publisher.

Winarni, Tri Indah A Single Common Assay for Robust and Rapid Fragile X Mental Retardation Syndrome Screening From Dried Blood Spots. Frontier.

Winarni, Tri Indah Subtelomeric chromosomal rearrangements in a large cohort of unexplained intellectually disabled individuals in 1 Indonesia: A clinical and molecular study. Indian Journal of Human Genetics.

Winarni, Tri Indah and Mundhofir, Farmaditya EP and Faradz, Sultana M.H. (2010) The Role of SHOX Gene in Short Stature of Turner Syndrome and Its Variant. Media Medika Indonesiana, 44 (2). pp. 57-61. ISSN 0126-1762

Winarni, Tri Indah and Sumekar, Tanjung Ayu and Belladonna, Maria and Mundhofir, Farmaditya EP and Faradz, Sultana M.H. (2013) Sindrom tremor dan ataksia terkait fragile X (FXTAS) : Risiko laki-laki pembawa sifat sindrom fragile X. NEURONA : Majalah Kedokteran Neuro-Sains Perhimpunan Dokter Spesialis Saraf Indonesia, 31 (1). pp. 1-9. ISSN 0216-6412

This list was generated on Fri Dec 6 17:34:04 2019 WIT.