DELETION OF THE SHORT ARM OF CHROMOSOME-20 IN ARTERIOHEPATIC DYSPLASIA (ALAGILLE SYNDROME)

被引：0
|
作者：
HADCHOUEL, M
ZHANG, FR
AURIAS, A
DELEUZE, JF
DUTRILLAUX, AM
ALAGILLE, D
THOMAS, G
机构：
[1] HOP BICETRE,INSERM,U56,F-94270 KREMLIN BICETRE,FRANCE
[2] HOP BICETRE,HEPATOL PEDIAT,F-94270 KREMLIN BICETRE,FRANCE
[3] INST CURIE,GENET MOLEC TUMEURS LAB,F-75231 PARIS 05,FRANCE
来源：
HEPATOLOGY | 1989年 / 10卷 / 04期
关键词：
D O I：
暂无
中图分类号：
R57 [消化系及腹部疾病];
学科分类号：
摘要：
引用
收藏
页码：603 / 603
页数：1
相关论文
共 50 条
  • [21] A NEW CENTROMERIC HETEROMORPHISM IN THE SHORT ARM OF CHROMOSOME-20
    FRYNS, JP
    KLECZKOWSKA, A
    SMEETS, E
    VANDENBERGHE, H
    JOURNAL OF MEDICAL GENETICS, 1988, 25 (09) : 636 - 637
  • [22] PICTURE OF THE MONTH - ALAGILLE-SYNDROME (ARTERIOHEPATIC DYSPLASIA)
    MARODI, L
    RIGO, G
    KAPOSZTA, R
    ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 1994, 148 (03): : 287 - 288
  • [23] Middle Aortic Syndrome in a Boy with Arteriohepatic Dysplasia (Alagille Syndrome)
    A.G. Shefler
    M.K.H. Chan
    I. Ostman-Smith
    Pediatric Cardiology, 1997, 18 : 232 - 234
  • [24] Scintigraphic progress of the liver in a patient with Alagille syndrome (arteriohepatic dysplasia)
    Megumi Jinguji
    Shinsaku Tsuchimochi
    Masayuki Nakajo
    Hiroyuki Hamada
    Takuro Kamiyama
    Tomokazu Umanodan
    Atsushi Tani
    Yoshiaki Nakabeppu
    Tatsuru Kaji
    Hideo Takamatsu
    Hironori Haga
    Annals of Nuclear Medicine, 2003, 17 : 693 - 697
  • [25] Scintigraphic progress of the liver in a patient with Alagille syndrome (arteriohepatic dysplasia)
    Jinguji, M
    Tsuchimochi, S
    Nakajo, M
    Hamada, H
    Kamiyama, T
    Umanodan, T
    Tani, A
    Nakabeppu, Y
    Kaji, T
    Takamatsu, H
    Haga, H
    ANNALS OF NUCLEAR MEDICINE, 2003, 17 (08) : 693 - 697
  • [26] ELECTROPHYSIOLOGICAL FINDINGS IN A FAMILY WITH CONGENITAL ARTERIOHEPATIC DYSPLASIA (ALAGILLE SYNDROME)
    TANINO, T
    ISHIHARA, A
    NAGANUMA, K
    NAKAHATA, T
    DOCUMENTA OPHTHALMOLOGICA, 1986, 63 (01) : 83 - 89
  • [27] THE PROGNOSTIC-SIGNIFICANCE OF DELETION OF THE LONG ARM OF CHROMOSOME-20 IN MYELOID DISORDERS
    CAMPBELL, LJ
    GARSON, OM
    LEUKEMIA, 1994, 8 (01) : 67 - 71
  • [28] ABSENCE OF AN INTERSTITIAL DELETION IN THE SHORT ARM OF CHROMOSOME-20 IN PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-2
    IKEUCHI, T
    TAKAI, S
    MIKI, T
    TATEISHI, H
    NISHISHO, I
    KONDO, I
    JAPANESE JOURNAL OF HUMAN GENETICS, 1986, 31 (02): : 143 - 144
  • [29] PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME-20 - 46,XX,DEL(20)(P11)/46,XX MOSAICISM
    SILENGO, MC
    BELL, GL
    BIAGIOLI, M
    FRANCESCHINI, P
    CLINICAL GENETICS, 1988, 33 (02) : 108 - 110
  • [30] DELETION OF LONG ARM OF CHROMOSOME-20 [DEL(20)(Q11)] IN MYELOID DISORDERS
    TESTA, JR
    KINNEALEY, A
    ROWLEY, JD
    GOLDE, DW
    POTTER, D
    BLOOD, 1978, 52 (05) : 868 - 877
12345