Search Results - "molecular genetics"

Neural Stem Cells in Drosophila: Molecular Genetic Mechanisms Underlying Normal Neural Proliferation and Abnormal Brain Tumor Formation by Nidhi Saini, Heinrich Reichert

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Quantitative and molecular genetics of child and adolescent mental health disorders: Recent advances, knowledge gaps and directions for future research by Henrik Larsson

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Molecular-genetic aspects of the endometrium state on the day of the tentative implantation window in women with recurrent miscarriage in the programs of assisted reproductive technologies by K. P. Golovatyuk, O. M. Nosenko, E. T. Makshayeva, D. Yu. Trofimov, A. E. Donnikov, V. V. Kolin

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Current ideas about molecular genetic subtypes of ovarian cancer: a personalized approach and a new platform for further research by A. Rybin

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Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria by Shuang Hu, Shiyue Mei, Ning Liu, Xiangdong Kong

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RhD-induced immunogenetic disparity between mother and fetus: medical importance and economic effect of using molecular genetic technology by A. G. Konopliannikov, A. N. Toropovskii, D. A. Viktorov, Yu. V. Myakisheva, R. F. Burganova, A. V. Solovyev, A. V. Kazakova, V. B. Marinovskaya

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Clinical, Immunological and Molecular-Genetic Description of Symptoms in Children with Autoimmune Polyglandular Syndrome Type 1: Description of a Case Series by Olga I. Krasnoperova, Elena N. Smirnova, Galina V. Chistousova

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Prenatal Three-Dimensional Ultrasound Detection of Adducted Thumbs in X-Linked Hydrocephaly: Two Case Reports with Molecular Genetic Studies by Edgardo Corral, Andres Barrios, Monica Isnard, Pascale Saugier-Veber, Sophie M. Fortier, Sarah Durrin, Waldo Sepulveda

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Molecular-genetic aspects of the endometrium state on the day of the tentative implantation window in women with recurrent miscarriage in the programs of assisted reproductive technologies by K. P. Golovatyuk, O. M. Nosenko, E. T. Makshayeva, D. Yu. Trofimov, A. E. Donnikov, V. V. Kolin

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Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing by Dong Wang, Min Gao, Kaihui Zhang, Ruifeng Jin, Yuqiang Lv, Yong Liu, Jian Ma, Ya Wan, Zhongtao Gai, Yi Liu

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Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients by Qiang Zhang, Qiang Zhang, Qiang Zhang, Qiang Zhang, Qiang Zhang, Qi Yang, Qi Yang, Qi Yang, Qi Yang, Fei Shen, Fei Shen, Fei Shen, Fei Shen, Linlin Wang, Linlin Wang, Linlin Wang, Linlin Wang, Jingsi Luo, Jingsi Luo, Jingsi Luo, Jingsi Luo

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Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene by Ji-Hee Yoon, Soojin Hwang, Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi

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Immunohistochemical and molecular genetic analysis of p 53 in oral squamous cell carcinoma (scc) in Hospital University Science Malaysia: a preliminary study by Karima Akool Al-Salihi, S. L. Ang, A. Azlina, M.S. Farini, H. Jaffar

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Molecular Genetic Epidemiology of an Emerging Antimicrobial-Resistant <i>Klebsiella pneumoniae</i> Clone (ST307) Obtained from Clinical Isolates in Central Panama by Virginia Núñez-Samudio, Gumercindo Pimentel-Peralta, Mellissa Herrera, Maydelin Pecchio, Johana Quintero, Iván Landires

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Molecular-genetic study of <i>SMN1</i> and <i>SMN2</i> genes associated with spinal muscular atrophy in individuals with infertility prior to in vitro fertilization by E. V. Kudryavtseva, O. V. Lagutina, V. V. Kovalev, S. S. Deryabina, I. A. Zakharova, A. Yu. Cherepennikova

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Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia by Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

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Molecular genetic investigation of hereditary breast and ovarian cancer patients in the Southern Transdanubian region: widening the mutation spectrum and searching for new pathogenic variants using next-generation methods by László Baráti, Anita Maász, Alexandra Mikó, Alexandra Mikó, Éva Bércesi, Sultan Al Kalbani, Judit Bene, Sebestyén Kovács, László Mangel, Kinga Hadzsiev

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Clinical features and molecular genetic investigation of infantile-onset ascending hereditary spastic paralysis (IAHSP) in two Chinese siblings caused by a novel splice site ALS2 variation by Qiang Zhang, Qi Yang, Jingsi Luo, Xunzhao Zhou, Shang Yi, Shuyin Tan, Zailong Qin

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Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3 by Shin-Wen Chen, Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Pei-Chen Wu, Yen-Ni Chen, Chen-Ju Lin, Wen-Ling Chen, Wayseen Wang

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Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene by Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Yi-Ning Su, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang

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