Works matching X chromosome abnormalities

Results: 751
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    Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan.

    Published in:
    Clinical Pediatric Endocrinology, 2015, v. 24, n. 4, p. 167, doi. 10.1297/cpe.24.167
    By:
    • Toshiaki Tanaka;
    • Yutaka Igarashi;
    • Keiichi Ozono;
    • Kenji Ohyama;
    • Masamichi Ogawa;
    • Hisao Osada;
    • Kazumichi Onigata;
    • Susumu Kanzaki;
    • Hitoshi Kohno;
    • Yoshiki Seino;
    • Hiroaki Takahashi;
    • Toshihiro Tajima;
    • Katsuhiko Tachibana;
    • Hiroyuki Tanaka;
    • Yoshikazu Nishi;
    • Tomonobu Hasegawa;
    • Keinosuke Fujita;
    • Tohru Yorifuji;
    • Reiko Horikawa;
    • Susumu Yokoya
    Publication type:
    Article
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    Unique Case Reports Associated with Ovarian Failure: Necessity of Two Intact X Chromosomes.

    Published in:
    Case Reports in Genetics, 2012, p. 1, doi. 10.1155/2012/640563
    By:
    • Kandukuri, Lakshmi Rao;
    • Padmalatha, Venkata;
    • Kanakavalli, Murthy;
    • Turlapati, Raseswari;
    • Swapna, Mangalipally;
    • Vidyadhari, Metuku;
    • Saranaya, Govindaraghavan;
    • Himaja, Kattera;
    • Deenadayal, Mamata;
    • Sethi, Bipin Kumar;
    • Deb, Prasun;
    • Gupta, Nalini;
    • Chakraborthy, Baidyanath;
    • Nallari, Pratibha;
    • Singh, Lalji
    Publication type:
    Article
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    Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome.

    Published in:
    Arthritis & Rheumatology, 2017, v. 69, n. 11, p. 2187, doi. 10.1002/art.40207
    By:
    • Sharma, Rohan;
    • Harris, Valerie M.;
    • Cavett, Joshua;
    • Kurien, Biji T.;
    • Liu, Ke;
    • Koelsch, Kristi A.;
    • Fayaaz, Anum;
    • Chaudhari, Kaustubh S.;
    • Radfar, Lida;
    • Lewis, David;
    • Stone, Donald U.;
    • Kaufman, C. Erick;
    • Li, Shibo;
    • Segal, Barbara;
    • Wallace, Daniel J.;
    • Weisman, Michael H.;
    • Venuturupalli, Swamy;
    • Kelly, Jennifer A.;
    • Pons‐Estel, Bernardo;
    • Jonsson, Roland
    Publication type:
    Article
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    Gonadoblastoma in Patients with Ullrich-Turner Syndrome.

    Published in:
    Pediatric & Developmental Pathology, 2015, v. 18, n. 2, p. 117, doi. 10.2350/14-08-1539-OA.1
    By:
    • ZELAYA, GABRIELA;
    • LÓPEZ MARTI, JESSICA M.;
    • MARINO, ROXANA;
    • GARCIA DE DÁVILA, MARIA T.;
    • GALLEGO, MARTA S.
    Publication type:
    Article
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    Cutaneous clues for diagnosing X-chromosomal disorders.

    Published in:
    Clinical Genetics, 2014, v. 85, n. 4, p. 328, doi. 10.1111/cge.12162
    By:
    • Vreeburg, M.;
    • Sallevelt, S.C.E.H.;
    • Stegmann, A.P.A.;
    • van Geel, M.;
    • Detisch, Y.J.H.A.;
    • Schrander‐Stumpel, C.T.R.M.;
    • van Steensel, M.A.M.;
    • Marcus‐Soekarman, D.
    Publication type:
    Article
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    Complex X chromosome rearrangement associated with multiorgan autoimmunity.

    Published in:
    Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0152-5
    By:
    • Haltrich, Irén;
    • Pikó, Henriett;
    • Pamjav, Horolma;
    • Somogyi, Anikó;
    • Völgyi, Antónia;
    • David, Dezső;
    • Beke, Artúr;
    • Garamvölgyi, Zoltán;
    • Kiss, Eszter;
    • Karcagi, Veronika;
    • Fekete, György
    Publication type:
    Article
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