Search Results - "Medical genetics

Incontinentia Pigmenti: A Case Report of Early Clinical Symptoms in a Lack of Family Inheritance Positive Result by Yuan F, Zhu FN, Liu XJ, Li J, Xu HT

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Pharmacogenetics of Breast Cancer Treatments: A Sub-Saharan Africa Perspective by Nthontho KC, Ndlovu AK, Sharma K, Kasvosve I, Hertz DL, Paganotti GM

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SLCO1B1 c.388A > G variant incidence and the severity of hyperbilirubinemia in Indonesian neonates by Radhian Amandito, Rinawati Rohsiswatmo, Michelle Halim, Vanessa Tirtatjahja, Amarila Malik

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Familial cases of subacute necrotizing encephalomyelopathy (Leigh syndrome) by E.V. Shishkina, T.N. Bazilevskaya, I.V. Novikova, I.V. Leonova, Yu.G. Astanina, I.I. Cheskidova, D.A. Maiseenko

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Familial cases of subacute necrotizing encephalomyelopathy (Leigh syndrome) by E.V. Shishkina, T.N. Bazilevskaya, I.V. Novikova, I.V. Leonova, Yu.G. Astanina, I.I. Cheskidova, D.A. Maiseenko

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Modeling and scheduling intelligent method\'s application in increasing hospitals\' efficiency by neda Darvish, Farzad Towhidkhah, Rasoul khyhti, Mahnaz Vaezi

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Autosomal dominant transmission of transient neonatal lactic acidosis: a case report by Emily B. Mardian, Matthew A. Lines, Care4Rare Consortium, Gregory P. Moore

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Contribution of ZBTB20 Polymorphisms to Esophageal Cancer Risk Among the Chinese Han Population by Yu S, Yuan G, Hu F, Li Y, Chen Z, Zhang R, Li P, Chen Z, Song J

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Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center by Shujuan Yan, Qiuxia Yu, Hang Zhou, Ruibin Huang, You Wang, Chunling Ma, Fei Guo, Fang Fu, Ru Li, Fucheng Li, Xiangyi Jin, Li Zhen, Min Pan, Dongzhi Li, Can Liao

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DIFFERENTIAL DIAGNOSIS OF PROGENIC FORMS OF BITE AND ITS IMPORTANCE IN PREDICTING THE RESULTS OF ORTHODONTIC TREATMENT by P.S. Flis, K.V. Storozhenko

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Prenatal Diagnosis of a Fetus with Partial Duplication and Deletion of Chromosome 18 Due to Maternal Pericentric Inversion 18 by Manuel Alejandro Vásquez Salguero, Wilmar Saldarriaga Gil

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Study protocol for the Australian autism biobank: an international resource to advance autism discovery research by Gail A. Alvares, Paul A. Dawson, Cheryl Dissanayake, Valsamma Eapen, Jacob Gratten, Rachel Grove, Anjali Henders, Helen Heussler, Lauren Lawson, Anne Masi, Emma Raymond, Felicity Rose, Leanne Wallace, Naomi R. Wray, Andrew J. O. Whitehouse, the Australian Autism Biobank team

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Ferroptosis-Related APOE, BCL3 and ALOX5AP Gene Polymorphisms are Associated with the Risk of Thyroid Cancer by Xiao Z, Zhao H

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Advances in Microfluidics Technology for Diagnostics and Detection

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Toxin and Immunotoxin Based Therapeutic Approaches

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Comparative Studies of the Chromosomal Arrangement in the C-Metaphase Between Normal Karyotype and Trisomy-21 by D.D. Farhud, P. Mehdipour, M.P. Baur, E. Korn, G. Schwanitz

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Folliculocentric lymphocytic hypersensitivity reactions in CLL/SLL patients: A unique clinicopathologic entity amongst non‐specific hypersensitivity reactions by James Abbott, Jessica Corean, Ashley M. Snyder, Scott R. Florell, Rodney Miles, Deborah Stephens, David A. Wada

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Breast cancer as a significant social problem by Jakub Husejko, Mateusz Porada, Daria Bieniek, Natalia Skierkowska, Monika Prylińska, Nastazja Ruszkowska, Agnieszka Nawrocka, Justyna Sępka, Natalia Szczesna, Pamela Swierczek, Julianna Pałka, Kornelia Kędziora-Kornatowska

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Case Report: A Rare Cause of Ischemic Stroke in the Intensive Care Unit: Venous Sinus Thrombosis by Cem Ece, Şeyda Canlı, Fatih Balaban, Deniz Aslan, Duygu Engin

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Polymorphism of genes of hemostasis system, endothelial dysfunction and regulation of blood pressure in pregnant woman with preeclampsia and fetal growth retardation by T. O. Loskutova

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