HYPERPROLINEMIA AND PSYCHIATRY IN 22Q11.2 DELETION SYNDROME

被引:0
|
作者
van Asbeck, E. [1 ,2 ]
Morava-Kozicz, E. [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, NL-6525 ED Nijmegen, Netherlands
[2] Tulane Univ, New Orleans, LA 70118 USA
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
155
引用
收藏
页码:454 / 454
页数:1
相关论文
共 50 条
  • [31] Neurological manifestation of 22q11.2 deletion syndrome
    Michael Bayat
    Allan Bayat
    Neurological Sciences, 2022, 43 : 1695 - 1700
  • [32] Surgical Considerations in 22Q11.2 Deletion Syndrome
    Kirschner, Richard E.
    Baylis, Adriane L.
    CLINICS IN PLASTIC SURGERY, 2014, 41 (02) : 271 - +
  • [33] Molecular genetics of 22q11.2 deletion syndrome
    Morrow, Bernice E.
    McDonald-McGinn, Donna M.
    Emanuel, Beverly S.
    Vermeesch, Joris R.
    Scambler, Peter J.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (10) : 2070 - 2081
  • [34] EMOTION DYSREGULATION IN 22Q11.2 DELETION SYNDROME
    Campbell, L. E.
    Swaab, L.
    McCabe, K.
    Simon, T.
    JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2018, 62 (08) : 666 - 666
  • [35] Otorhinologic Disorders in 22q11.2 Deletion Syndrome
    Lu, Nathan
    Kacin, Alexa J. J.
    Shaffer, Amber D. D.
    Stapleton, Amanda L. L.
    OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2023, 169 (04) : 1012 - 1019
  • [36] FISH Diagnosis of 22q11.2 Deletion Syndrome
    Miller, Kimberley A.
    NEWBORN AND INFANT NURSING REVIEWS, 2008, 8 (01) : E11 - E19
  • [37] OCULAR FINDINGS IN 22Q11.2 DELETION SYNDROME
    Gokturk, Bahar
    Bozkurt, Banu
    Yildirim, Mahmut Selman
    Reisli, Ismail
    JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 (06) : 735 - 736
  • [38] Neurobiological perspective of 22q11.2 deletion syndrome
    Zinkstok, Janneke R.
    Boot, Erik
    Bassett, Anne S.
    Hiroi, Noboru
    Butcher, Nancy J.
    Vingerhoets, Claudia
    Vorstman, Jacob A. S.
    van Amelsvoort, Therese A. M. J.
    LANCET PSYCHIATRY, 2019, 6 (11): : 951 - 960
  • [39] The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
    Du, Qiumei
    de la Morena, M. Teresa
    van Oers, Nicolai S. C.
    FRONTIERS IN GENETICS, 2020, 10
  • [40] Clinical Manifestations of 22q11.2 Deletion Syndrome
    Cirillo, Annapaola
    Lioncino, Michele
    Maratea, Annachiara
    Passariello, Annalisa
    Fusco, Adelaide
    Fratta, Fiorella
    Monda, Emanuele
    Caiazza, Martina
    Signore, Giovanni
    Esposito, Augusto
    Baban, Anwar
    Versacci, Paolo
    Putotto, Carolina
    Marino, Bruno
    Pignata, Claudio
    Cirillo, Emilia
    Giardino, Giuliana
    Sarubbi, Berardo
    Limongelli, Giuseppe
    Russo, Maria Giovanna
    HEART FAILURE CLINICS, 2022, 18 (01) : 155 - 164