Isochromosome 1q in congenital oronasopharyngeal teratoma (epignathus)

被引:0
|
作者
Brink, David [1 ]
Gapp, Joshua [1 ]
Batanian, Jacqueline R. [1 ]
机构
[1] St Louis Univ, Sch Med, St Louis, MO USA
关键词
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
487
引用
收藏
页码:106 / 106
页数:1
相关论文
共 50 条
  • [21] TERMINAL DELETION WITH STABLE ACENTRIC FRAGMENT OF 1Q IN A CHILD WITH CONGENITAL-MALFORMATIONS
    KUCEROVA, M
    POLIVKOVA, Z
    DLUHOLUCKY, S
    KVASNICOVA, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 1983, 35 (01) : 91 - 95
  • [22] Triplication of 1q in Fanconi anemia
    Ferro, MT
    Vazquez-Mazariego, Y
    Ramiro, S
    Sanchez-Hombre, MC
    Villalon, C
    Garcia-Sagredo, JM
    Ulibarrena, C
    Sastre, JL
    San Roman, C
    CANCER GENETICS AND CYTOGENETICS, 2001, 127 (01) : 38 - 41
  • [23] Complement component 1q in glucotoxicity
    Engin, A. B.
    Karakus, R.
    TOXICOLOGY LETTERS, 2015, 238 (02) : S225 - S225
  • [24] Novartis reports strong 1Q
    Chemical Market Reporter, 2003, 263 (16):
  • [25] Is schizophrenia linked to chromosome 1q?
    Macgregor, S
    Visscher, PM
    Knott, S
    Porteous, D
    Muir, W
    Millar, K
    Blackwood, D
    SCIENCE, 2002, 298 (5602) : 2277 - 2277
  • [26] Multiple congenital malformations in an infant prenatally diagnosed with mosaicism for dup(1q) and del(Xq)
    Wells, SR
    Kuller, JA
    Rao, KW
    Aylsworth, AS
    CLINICAL GENETICS, 1996, 49 (04) : 216 - 219
  • [27] CASE OF PARTIAL TRISOMY 1Q
    KIMURA, S
    NARAHARA, K
    KODAMA, Y
    KIMOTO, H
    JAPANESE JOURNAL OF HUMAN GENETICS, 1979, 24 (03): : 159 - 160
  • [28] Congenital diaphragmatic hernia with a pure duplication of chromosome 1q: report of the first surviving case
    Kohei Otake
    Keiichi Uchida
    Mikihiro Inoue
    Yuhki Koike
    Kohei Matsushita
    Chikao Miki
    Takashi Sugiyama
    Masato Kusunoki
    Pediatric Surgery International, 2009, 25 : 827 - 831
  • [29] Congenital diaphragmatic hernia with a pure duplication of chromosome 1q: report of the first surviving case
    Otake, Kohei
    Uchida, Keiichi
    Inoue, Mikihiro
    Koike, Yuhki
    Matsushita, Kohei
    Miki, Chikao
    Sugiyama, Takashi
    Kusunoki, Masato
    PEDIATRIC SURGERY INTERNATIONAL, 2009, 25 (09) : 827 - 831
  • [30] A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q
    Della Monica, Matteo
    Lonardo, Fortunato
    Faravelli, Francesca
    Pierluigi, Mauro
    Luquetti, Daniela Varela
    De Gregori, Manuela
    Zuffardi, Orsetta
    Scarano, Gioacchirio
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2007, 143A (22) : 2733 - 2737