Search Results - "Medical genetics

Correction to: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report by Maryam Sobhani, Mohammad Amin Tabatabaiefar, Soudeh Ghafouri-Fard, Asadollah Rajab, Asal Hojjat, Abdol-Mohammad Kajbafzadeh, Mohammad Reza Noori-Daloii

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Associations Among Disseminated Intravascular Coagulation, Thrombocytopenia Cytokines/Chemokines and Genetic Polymorphisms of Toll-Like Receptor 2/4 in Chinese Patients with Sepsis by Jiang S, Ma J, Ye S, Meaney C, Moore TE, Pan S, Gao C

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Association of vitamin D receptor TaqI and ApaI genetic polymorphisms with nephrolithiasis and end stage renal disease: a meta-analysis by Tajamul Hussain, Shaik M. Naushad, Anwar Ahmed, Salman Alamery, Arif A. Mohammed, Mohamed O. Abdelkader, Nasser Abobakr Nasser Alkhrm

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Lack of association between genetic polymorphisms within <it>DUSP12 - </it><it>ATF6 </it>locus and glucose metabolism related traits in a Chinese population by Xiang Kunsan, Bao Yuqian, Wang Jie, Ma Xiaojing, Wang Congrong, Zhang Rong, Hu Cheng, Jia Weiping

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Healthy Baby Born to a Robertsonian Translocation Carrier following Next-Generation Sequencing-Based Preimplantation Genetic Diagnosis: A Case Report by Krzysztof Lukaszuk, Sebastian Pukszta, Karolina Ochman, Celina Cybulska, Joanna Liss, Ewa Pastuszek, Judyta Zabielska, Izabela Woclawek-Potocka

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A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran by Yeganeh Keshvar, Solmaz Sabeghi, Zohreh Sharifi, Kiyana Sadat Fatemi, Panti Fouladi, Shahrzad Younesi Khah, Faezeh Rahiminejad, Atefeh Joudaki, Masoume Amini, Hamideh Bagherian, Marefat Ghaffari Novin, Mansoureh Movahedin, Marzieh Mojbafan, Sirous Zeinali

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Designation and psychometric properties of the Short Form Postpartum Quality of Life Questionnaire (SF-PQOL): an application of multidimensional item response theory and genetic al... by Fariba Nikan, Mohammad Asghari Jafarabadi, Sakineh Mohammad-Al, Mojgan Mirghafourvand

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Absence of association between <it>SERPINE2 </it>genetic polymorphisms and chronic obstructive pulmonary disease in Han Chinese: a case-control cohort study by Sun Chang, Fu Wei-Ping, Zhong Li, Dai Lu-Ming, Zhang Ya-Ping

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A clinical case of atopic dermatitis with a rapid positive effect from the use of a genetically engineered biological drug in a teenager by E. V. Churyukina, E. A. Portnyaga

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Predictors of Intention to Consume Genetically Modified Oil among Personnel of Community Health Care Centers in Yazd, Iran: An Application of the Theory of Planned Behavior by Masoumeh Abbasishavazi, Bahador Hajimohammadi, Zahra Hajebrahimi

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Role of genetic variations and protein expression of β-Microsemino protein in intrauterine insemination outcome of unexplained infertile men: A case-control study by Elham Bagherian, Sahar Jokari, Parnaz Borjian Boroujeni, Kaveh Haratian, Marjan Sabbaghian, Anahita Mohseni Meybodi

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Association between serotonin 2A receptor (HTR2A) genetic variations and risk of hypertension in a community-based cohort study by Jung Ran Choi, Minhee Jeon, Sang Baek Koh

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IKZF1 genetic variants rs4132601 and rs11978267 and acute lymphoblastic leukemia risk in Tunisian children: a case-control study by Sana Mahjoub, Vera Chayeb, Hedia Zitouni, Rabeb M. Ghali, Haifa Regaieg, Wassim Y. Almawi, Touhami Mahjoub

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Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases by Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Farzad Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad-Reza Ghasemi

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Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China by Shan Wu, Zhidan Wu, Manlian Chen, Xiangbin Zhong, Haoyan Gu, Wenjing Du, Weidong Liu, Li Lang, Junyi Wang

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A healthy live birth after mosaic blastocyst transfer in preimplantation genetic testing for GATA1-related cytopenia combined with HLA matching by Huiling Xu, Jiajie Pu, Zhengzhong Wu, Yulong Huang, Chanlin Han, Xuemei Li

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Prediction of metabolic syndrome using machine learning approaches based on genetic and nutritional factors: a 14-year prospective-based cohort study by Dayeon Shin

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Genetic analysis of children with congenital ocular anomalies in three ecological regions of Nepal: a phase II of Nepal pediatric ocular diseases study by Srijana Adhikari, Neelam Thakur, Ujjowala Shrestha, Mohan K Shrestha, Murarai Manshrestha, Bijay Thapa, Manish Poudel, Ajaya Kunwar

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Do the mutations of <it>C1GALT1C1 </it>gene play important roles in the genetic susceptibility to Chinese IgA nephropathy? by LV Ji-Cheng, Zhang Hong, Nie Guang-Jun, Li Gui-Sen, Shen Yan, Wang Hai-Yan

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Autism genetic database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites by Talebizadeh Zohreh, Matuszek Gregory

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