PROBLEMS IN THE DETECTION OF 15Q DELETION IN PATIENTS WITH PRADER-WILLI SYNDROME

被引：0
|
作者：
WYANDT, HE
PATIL, S
SHAH, HO
HANSON, JW
ZELLWEGER, H
KELLY, TE
DOLAN, LM
WILSON, WG
机构：
[1] UNIV VIRGINIA,DEPT PEDIAT,CHARLOTTESVILLE,VA 22903
[2] UNIV IOWA,HOSP & CLIN,IOWA CITY,IA 52240
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1981年 / 33卷 / 06期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：A127 / A127
页数：1
相关论文
共 50 条
  • [21] CHROMOSOME-15 DELETION IN THE PRADER-WILLI SYNDROME
    FORD, JH
    SHEFFIELD, LJ
    WHITE, DI
    PATHOLOGY, 1983, 15 (01) : 104 - 104
  • [22] A special case of Prader-Willi syndrome with 15q11-q13 deletion
    Gorduza, E.
    Rusu, C.
    Braha, E.
    Gramescu, M.
    Bujoran, C.
    Ivanov, I.
    Covic, M.
    CHROMOSOME RESEARCH, 2009, 17 : 58 - 59
  • [23] Molecular and clinical characterization of two patients with Prader-Willi syndrome and atypical deletions of proximal chromosome 15q
    Calounova, Gabriela
    Hedvicakova, Petra
    Silhanova, Eva
    Kreckova, Gabriela
    Sedlacek, Zdenek
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (15) : 1955 - 1962
  • [24] Clinical evaluation of Prader-Willi and Angelman syndrome patients with 15q11-13 deletion
    Kurtul
    Boduroglu, K.
    Alanay, Y.
    Utine, E.
    Salanci, B. Volkan
    Aktas, D.
    Alikasifoglu, M.
    Tuncbilek, E.
    CHROMOSOME RESEARCH, 2007, 15 : 96 - 96
  • [25] 无典型Prader-Willi表型的15q中间缺失
    曾建华
    国际遗传学杂志, 1991, (05) : 280 - 280
  • [26] Maternal chromosome 15 deletion in a case of Prader-willi syndrome
    Batstone, Paul
    Forsyth, L. A.
    Cooke, A.
    JOURNAL OF MEDICAL GENETICS, 2008, 45 : S92 - S92
  • [27] PRADER-WILLI SYNDROME ASSOCIATED WITH AN INTERSTITIAL DELETION OF CHROMOSOME 15
    BONUCCELLI, CM
    STETTEN, G
    LEVITT, RC
    LEVIN, LS
    PYERITZ, RE
    JOHNS HOPKINS MEDICAL JOURNAL, 1982, 151 (05): : 237 - 242
  • [28] PHENOTYPIC DIFFERENCES BETWEEN PATIENTS WITH PRADER-WILLI-SYNDROME DUE TO DELETION 15Q AND UNIPARENTAL DISOMY-15
    CASSIDY, SB
    FORSYTHE, M
    HEEGER, S
    NICHOLLS, RD
    SCHWARTZ, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 88 - 88
  • [29] An Interstitial 15q11-q14 Deletion: Expanded Prader-Willi Syndrome Phenotype
    Butler, Merlin G.
    Bittel, Douglas C.
    Kibiryeva, Nataliya
    Cooley, Linda D.
    Yu, Shihui
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (02) : 404 - 408
  • [30] Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region
    Butler, MG
    Bittel, D
    Talebizadeh, Z
    JOURNAL OF MEDICAL GENETICS, 2002, 39 (03) : 202 - 204
12345