Works in Molecular Genetics & Genomic Medicine, 2020, Vol 8, Issue 9

Results: 63
    1

    Issue Information.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.766
    Publication type:
    Article
    2

    Cover.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1511
    By:
    • Morales‐Rosado, Joel A.;
    • Macke, Erica L.;
    • Cousin, Margot A.;
    • Oliver, Gavin R.;
    • Dhamija, Radhika;
    • Klee, Eric W.
    Publication type:
    Article
    3

    Cover.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1510
    By:
    • Liao, Yu‐Huang;
    • Teng, Ming‐Sheng;
    • Juang, Jyh‐Ming J.;
    • Chiang, Fu‐Tien;
    • Er, Leay‐Kiaw;
    • Wu, Semon;
    • Ko, Yu‐Lin
    Publication type:
    Article
    4
    5
    6

    An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1408
    By:
    • Rasool, Sajida;
    • Baig, Jamshaid Mahmood;
    • Moawia, Abubakar;
    • Ahmad, Ilyas;
    • Iqbal, Maria;
    • Waseem, Syeda Seema;
    • Asif, Maria;
    • Abdullah, Uzma;
    • Makhdoom, Ehtisham Ul Haq;
    • Kaygusuz, Emrah;
    • Zakaria, Muhammad;
    • Ramzan, Shafaq;
    • Haque, Saif ul;
    • Mir, Asif;
    • Anjum, Iram;
    • Fiaz, Mehak;
    • Ali, Zafar;
    • Tariq, Muhammad;
    • Saba, Neelam;
    • Hussain, Wajid
    Publication type:
    Article
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17

    Aberrant X chromosomal rearrangement through multi‐step template switching during sister chromatid formation in a patient with severe hemophilia A.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1390
    By:
    • Tokoro, Mahiru;
    • Tamura, Shogo;
    • Suzuki, Nobuaki;
    • Kakihara, Misaki;
    • Hattori, Yuna;
    • Odaira, Koya;
    • Suzuki, Sachiko;
    • Takagi, Akira;
    • Katsumi, Akira;
    • Hayakawa, Fumihiko;
    • Okamoto, Shuichi;
    • Suzuki, Atsuo;
    • Kanematsu, Takeshi;
    • Matsushita, Tadashi;
    • Kojima, Tetsuhito
    Publication type:
    Article
    18
    19

    Rare variants in the GABA<sub>A</sub> receptor subunit ε identified in patients with a wide spectrum of epileptic phenotypes.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1388
    By:
    • Markus, Fenja;
    • Angelini, Chloé;
    • Trimouille, Aurelien;
    • Rudolf, Gabrielle;
    • Lesca, Gaetan;
    • Goizet, Cyril;
    • Lasseaux, Eulalie;
    • Arveiler, Benoit;
    • Slegtenhorst, Marjon;
    • Brooks, Alice S.;
    • Abou Jamra, Rami;
    • Korenke, Georg‐Christoph;
    • Neidhardt, John;
    • Owczarek‐Lipska, Marta
    Publication type:
    Article
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30
    31

    Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1363
    By:
    • Hamdaoui, Hasna;
    • Benlarroubia, Oumaima;
    • Ait Boujmia, Oum Kaltoum;
    • Mossafa, Hossein;
    • Ouldim, Karim;
    • Belkhayat, Aziza;
    • Smyej, Imane;
    • Benrahma, Houda;
    • Dehbi, Hind;
    • Chegdani, Fatima
    Publication type:
    Article
    32
    33
    34
    35

    FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1373
    By:
    • Cucinotta, Francesca;
    • Ricciardello, Arianna;
    • Turriziani, Laura;
    • Calabrese, Giorgia;
    • Briguglio, Marilena;
    • Boncoddo, Maria;
    • Bellomo, Fabiana;
    • Tomaiuolo, Pasquale;
    • Martines, Silvia;
    • Bruschetta, Marianna;
    • La Fauci Belponer, Francesca;
    • Di Bella, Tiziana;
    • Colombi, Costanza;
    • Baccarin, Marco;
    • Picinelli, Chiara;
    • Castronovo, Paola;
    • Lintas, Carla;
    • Sacco, Roberto;
    • Biederer, Thomas;
    • Kellam, Barbara
    Publication type:
    Article
    36
    37
    38
    39
    40
    41
    42
    43
    44
    45

    Genetic alteration of colorectal adenoma‐carcinoma sequence among gastric adenocarcinoma and dysplastic lesions in a patient with attenuated familial adenomatous polyposis.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1348
    By:
    • Tanabe, Hiroki;
    • Moriichi, Kentaro;
    • Takahashi, Keitaro;
    • Ono, Yusuke;
    • Kobayashi, Yu;
    • Murakami, Yuki;
    • Iwama, Takuya;
    • Kunogi, Takehito;
    • Sasaki, Takahiro;
    • Ando, Katsuyoshi;
    • Ueno, Nobuhiro;
    • Kashima, Shin;
    • Takei, Hidehiro;
    • Mizukami, Yusuke;
    • Fujiya, Mikihiro;
    • Okumura, Toshikatsu
    Publication type:
    Article
    46
    47
    48
    49
    50