A CASE OF THE PRADER-WILLI SYNDROME HAVING THE INTERSTITIAL DELETION OF NO 15 CHROMOSOME

被引:2
|
作者
KADOTANI, T
WATANABE, Y
KANATA, S
KUMADA, T
TAKEMURA, I
机构
[1] KAMO NATL SANATORIUM,DEPT PSYCHIAT,HIROSHIMA,JAPAN
[2] KOJIKA GAKUEN,HIROSHIMA,JAPAN
关键词
D O I
10.2183/pjab.62.405
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
引用
收藏
页码:405 / 407
页数:3
相关论文
共 50 条
  • [41] Prader-Willi syndrome: report of a case
    Hasnaa, A.
    Daniela, N.
    Lamiaa, H.
    Asmaa, C.
    Siham, E.
    Hassan, E.
    Ahmed, F.
    DIABETES & METABOLISM, 2012, 38 : A124 - A124
  • [42] Prader-Willi syndrome - case report
    Stodulska-Blaszke, Aldona
    Wojcicka, Anna
    FAMILY MEDICINE AND PRIMARY CARE REVIEW, 2012, 14 (03): : 531 - 533
  • [43] Prader-Willi syndrome: Case report
    Lupi, Omar
    de Castro Dani, Christiane Maria
    Aguiar, Ericka
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2009, 60 (03) : AB46 - AB46
  • [44] PRADER-WILLI SYNDROME ASSOCIATED WITH INV(15)
    WINSOR, EJT
    WELCH, JP
    RAFTUS, RA
    AMERICAN JOURNAL OF HUMAN GENETICS, 1982, 34 (06) : A151 - A151
  • [45] A RARE CASE OF PRADER-WILLI SYNDROME
    Akshar, Patel
    Bharat, Patel
    JOURNAL OF INVESTIGATIVE MEDICINE, 2017, 65 (02) : 526 - 526
  • [46] The syndrome of Prader-Willi (A case report)
    Drissi Touzani, K.
    Marrakchi, M.
    Chraibi, F.
    Abdellaoui, M.
    Benatiya Andaloussi, I.
    Tahiri, H.
    JOURNAL FRANCAIS D OPHTALMOLOGIE, 2018, 41 (04): : E165 - E166
  • [47] CLINICAL DIFFERENCES BETWEEN CHROMOSOME 15Q DELETION AND NON DELETION PRADER-WILLI INDIVIDUALS
    BUTLER, MG
    MEANEY, FJ
    KALER, SG
    YU, PL
    PALMER, CG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1982, 34 (06) : A119 - A119
  • [48] Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15
    L'Herminé, AC
    Aboura, A
    Brisset, S
    Cuisset, L
    Castaigne, V
    Labrune, P
    Frydman, R
    Tachdjian, G
    PRENATAL DIAGNOSIS, 2003, 23 (11) : 938 - 943
  • [49] Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities
    Muralidhar, B
    Marney, A
    Butler, MG
    GENETICS IN MEDICINE, 1999, 1 (04) : 141 - 145
  • [50] PRADER-WILLI SYNDROME AND CHROMOSOME-15 - A CLINICAL DISCUSSION OF 20 CASES
    MATTEI, JF
    MATTEI, MG
    GIRAUD, F
    HUMAN GENETICS, 1983, 64 (04) : 356 - 362