Works matching IS 20734425 AND DT 2020 AND VI 11 AND IP 12


Results: 140
    1
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11

    The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein.

    Published in:
    Genes, 2020, v. 11, n. 12, p. 1519, doi. 10.3390/genes11121519
    By:
    • Laforgia, Nicola;
    • De Cosmo, Lucrezia;
    • Palumbo, Orazio;
    • Ranieri, Carlotta;
    • Sesta, Michela;
    • Capodiferro, Donatella;
    • Pantaleo, Antonino;
    • Iapicca, Pierluigi;
    • Lastella, Patrizia;
    • Capozza, Manuela;
    • Schettini, Federico;
    • Bukvic, Nenad;
    • Bagnulo, Rosanna;
    • Resta, Nicoletta
    Publication type:
    Article
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38
    39
    40
    41
    42
    43
    44
    45

    Karyotype Evolution in 10 Pinniped Species: Variability of Heterochromatin versus High Conservatism of Euchromatin as Revealed by Comparative Molecular Cytogenetics.

    Published in:
    Genes, 2020, v. 11, n. 12, p. 1485, doi. 10.3390/genes11121485
    By:
    • Beklemisheva, Violetta R.;
    • Perelman, Polina L.;
    • Lemskaya, Natalya A.;
    • Proskuryakova, Anastasia A.;
    • Serdyukova, Natalya A.;
    • Burkanov, Vladimir N.;
    • Gorshunov, Maksim B.;
    • Ryder, Oliver;
    • Thompson, Mary;
    • Lento, Gina;
    • O'Brien, Stephen J.;
    • Graphodatsky, Alexander S.
    Publication type:
    Article
    46
    47
    48
    49
    50