1q21.1 Deletions and Duplications in 2 Siblings with Psychiatric Problems

被引:3
|
作者
Kaymakcalan, Hande [1 ]
Li, Peining [2 ]
机构
[1] Demiroglu Bilim Univ, Dept Pediat, Pediat Genet Unit, Istanbul, Turkey
[2] Yale Univ, Dept Clin Genet, New Haven, CT USA
来源
INDIAN JOURNAL OF PEDIATRICS | 2019年 / 86卷 / 11期
关键词
D O I
10.1007/s12098-019-03014-2
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:1068 / 1068
页数:1
相关论文
共 50 条
  • [1] 1q21.1 Deletions and Duplications in 2 Siblings with Psychiatric Problems
    Hande Kaymakçalan
    Peining Li
    The Indian Journal of Pediatrics, 2019, 86 : 1068 - 1068
  • [2] Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1
    Pang, Hui
    Yu, Xiaowei
    Kim, Young Mi
    Wang, Xianfu
    Jinkins, Jeremy K.
    Yin, Jianing
    Li, Shibo
    Gu, Hongcang
    FRONTIERS IN GENETICS, 2020, 11
  • [3] Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
    Martina Busè
    Helenia C. Cuttaia
    Daniela Palazzo
    Marcella V. Mazara
    Salvatrice A. Lauricella
    Michela Malacarne
    Mauro Pierluigi
    Simona Cavani
    Maria Piccione
    Italian Journal of Pediatrics, 43
  • [4] Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series
    Buse, Martina
    Cuttaia, Helenia C.
    Palazzo, Daniela
    Mazara, Marcella V.
    Lauricella, Salvatrice A.
    Malacarne, Michela
    Pierluigi, Mauro
    Cavani, Simona
    Piccione, Maria
    ITALIAN JOURNAL OF PEDIATRICS, 2017, 43
  • [5] Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
    Nicola Brunetti-Pierri
    Jonathan S Berg
    Fernando Scaglia
    John Belmont
    Carlos A Bacino
    Trilochan Sahoo
    Seema R Lalani
    Brett Graham
    Brendan Lee
    Marwan Shinawi
    Joseph Shen
    Sung-Hae L Kang
    Amber Pursley
    Timothy Lotze
    Gail Kennedy
    Susan Lansky-Shafer
    Christine Weaver
    Elizabeth R Roeder
    Theresa A Grebe
    Georgianne L Arnold
    Terry Hutchison
    Tyler Reimschisel
    Stephen Amato
    Michael T Geragthy
    Jeffrey W Innis
    Ewa Obersztyn
    Beata Nowakowska
    Sally S Rosengren
    Patricia I Bader
    Dorothy K Grange
    Sayed Naqvi
    Adolfo D Garnica
    Saunder M Bernes
    Chin-To Fong
    Anne Summers
    W David Walters
    James R Lupski
    Pawel Stankiewicz
    Sau Wai Cheung
    Ankita Patel
    Nature Genetics, 2008, 40 : 1466 - 1471
  • [6] Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
    Brunetti-Pierri, Nicola
    Berg, Jonathan S.
    Scaglia, Fernando
    Belmont, John
    Bacino, Carlos A.
    Sahoo, Trilochan
    Lalani, Seema R.
    Graham, Brett
    Lee, Brendan
    Shinawi, Marwan
    Shen, Joseph
    Kang, Sung-Hae L.
    Pursley, Amber
    Lotze, Timothy
    Kennedy, Gail
    Lansky-Shafer, Susan
    Weaver, Christine
    Roeder, Elizabeth R.
    Grebe, Theresa A.
    Arnold, Georgianne L.
    Hutchison, Terry
    Reimschisel, Tyler
    Amato, Stephen
    Geragthy, Michael T.
    Innis, Jeffrey W.
    Obersztyn, Ewa
    Nowakowska, Beata
    Rosengren, Sally S.
    Bader, Patricia I.
    Grange, Dorothy K.
    Naqvi, Sayed
    Garnica, Adolfo D.
    Bernes, Saunder M.
    Fong, Chin-To
    Summers, Anne
    Walters, W. David
    Lupski, James R.
    Stankiewicz, Pawel
    Cheung, Sau Wai
    Patel, Ankita
    NATURE GENETICS, 2008, 40 (12) : 1466 - 1471
  • [7] 1q21.1 CNVs
    Grangeia, A.
    Pinto, J.
    Leao, M.
    Guimaraes, S.
    Ramalho, C.
    Oliveira, R.
    Doria, S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 452 - 452
  • [8] Rearrangement hot spot on 1q21.1
    不详
    NATURE GENETICS, 2008, 40 (10) : 1151 - 1151
  • [9] 1q21.1 Microduplication expression in adults
    Dolcetti, Alessia
    Silversides, Candice K.
    Marshall, Christian R.
    Lionel, Anath C.
    Stavropoulos, Dimitri J.
    Scherer, Stephen W.
    Bassett, Anne S.
    GENETICS IN MEDICINE, 2013, 15 (04) : 282 - 289
  • [10] 1q21.1 Duplication syndrome and epilepsy
    Gourari, Ioulia
    Schubert, Romaine
    Prasad, Aparna
    NEUROLOGY-GENETICS, 2018, 4 (01)