Search Results - "Molecular Genetics"

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  1. 361
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    POLG Novel Mutation with Alpers Syndrome by J Gordon Millichap

    Published 2012
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  2. 362
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    Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum by J Gordon Millichap

    Published 2003
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  3. 363
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    Angelman Syndrome: Molecular Cytogenetic Studies by J Gordon Millichap

    Published 1997
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  4. 364
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    Prioritization of genes involved in endothelial cell apoptosis by their implication in lymphedema using an analysis of associative gene networks with ANDSystem by Olga V. Saik, Vadim V. Nimaev, Dilovarkhuja B. Usmonov, Pavel S. Demenkov, Timofey V. Ivanisenko, Inna N. Lavrik, Vladimir A. Ivanisenko

    Published 2019
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  5. 365
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    Infantile Hypophosphatasia: Clinical Case by Tatyana V. Gabrusskaya, Yana V. Panutina, Maria O. Revnova, Mikhail M. Kostik

    Published 2020
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  6. 366
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    Hermansky-Pudlak Syndrome Type 6 Accompanied with Bowel Vascular Malformation: Clinical Case by Natalia V. Zhurkova, Nato D. Vashakmadze, Natella V. Suhanova, Grigorii V. Revunenekov, Olga B. Gordeeva, Maria V. Egorova, Dmitriy S. Ovchinnikov, Vitaliy V. Kadyshev, Rena A. Zhinchenko, Leyla S. Namazova-Baranova

    Published 2021
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  7. 367
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    The effect of <i>OPRM1, ABCB1, IL1B, PTGS2, LOC 541472</i> gene polymorphism on the variability of chronic pain syndrome in patients with pancreatic cancer by O. P. Bobrova, N. A. Schnider, S. K. Zyryanov, D V. Dmitrenko, S. N. Zobova, R. A. Zukov

    Published 2020
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  8. 368
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    Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Shin-Yu Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang

    Published 2020
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  9. 369
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    Age-related relationship between the development of hyperplastic processes and VEGF expression in endometrial cells by Z. V. Chumak, M. V. Shapoval, V. V. Artyomenko

    Published 2020
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  10. 370
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    DIAGNOSIS OF POSTOPERATIVE PELVIC ADHESIONS IN WOMEN WITH CHRONIC PELVIC PAIN ON THE BACKGROUND OF UNDIFFERENTIATED CONNECTIVE TISSUE DYSPLASIA by M. BEN SALKHA, N.B. REPINA, M.N. DMITRIEVA

    Published 2018
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  11. 371
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    A CLINICAL CASE OF OSTEOGENESIS IMPERFECT TYPE III, DETERMINED BY COL1A1 (P.GLY845ARG) GENE MUTATION IN A NEWBORN GIRL by І. Ластівка, В. Анцупова, А. Бабінцева, О. Юрків, Л. Брішевац, І. Малєєва

    Published 2022
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  12. 372
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    Angelman syndrome in two siblings: clinical case by Uliyana S. Suraeva, Olga M. Matyasova, Anna V. Monakhova, Alla Yu. Shutkova, Elena V. Tush, Elena E. Yatsyshina, Marina A. Suslova, Olga V. Khaletskaya

    Published 2023
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  13. 373
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    Pontocerebellar Hypoplasia Type 1 by J Gordon Millichap

    Published 2009
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  14. 374
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    X-Linked Charcot-Marie-Tooth Disease in 93 Patients by J Gordon Millichap

    Published 2001
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  15. 375
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    Migrating Partial Seizures of Infancy by J Gordon Millichap

    Published 2013
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  16. 376
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    Drug treatment for cancer of the corpus uteri: Protracted stagnation or breakthrough expectation by E. V. Artamonova

    Published 2014
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  17. 377
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    GENETIC ASPECTS OF CONGENITAL LONG QT SYNDROME by A. A. Chernova, S. Yu. Nikulina, A. V. Gul'bis

    Published 2015
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  18. 378
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    MLPA in the initial genetic screening of patients with acute myeloid leukemia by Yahya Dinnar, Hachmeriyan Mari, Ruseva Tsanka, Chervenkov Trifon, Micheva Ilina

    Published 2024
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  19. 379
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    Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations by Artur Beke, Henriett Piko, Iren Haltrich, Veronika Karcagi, Janos Rigo, Maria Judit Molnar, György Fekete

    Published 2018
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  20. 380
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    Role of gene polymorphism of IL-4 and IL-17 in recurrent miscarriage, came in art cycles by K. P. Golovatyuk

    Published 2017
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