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
  • [41] Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region.
    Butler, MG
    Bittel, DC
    Talebizadeh, Z
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 314 - 314
  • [42] RESTRICTION FRAGMENT LENGTH POLYMORPHISMS WITHIN PROXIMAL 15Q AND THEIR USE IN MOLECULAR CYTOGENETICS AND THE PRADER-WILLI SYNDROME
    NICHOLLS, RD
    KNOLL, JH
    GLATT, K
    HERSH, JH
    BREWSTER, TD
    GRAHAM, JM
    WURSTERHILL, D
    WHARTON, R
    LATT, SA
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 33 (01): : 66 - 77
  • [43] INTERSTITIAL-15Q DELETION WITHOUT A CLASSIC PRADER-WILLI PHENOTYPE
    GALAN, F
    AGUILAR, MS
    GONZALEZ, J
    CLEMENTE, F
    SANCHEZ, R
    TAPIA, M
    MOYA, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 38 (04): : 532 - 534
  • [44] CLINICAL COMPARISON OF 59 PRADER-WILLI PATIENTS WITH AND WITHOUT THE 15(Q12) DELETION
    WENGER, SL
    HANCHETT, JM
    STEELE, MW
    MAIER, BV
    GOLDEN, WL
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (04): : 881 - 887
  • [45] THE PRADER-WILLI SYNDROME AND INTERSTITIAL DELETION OF CHROMOSOME 15 - HIGH-RESOLUTION CHROMOSOME ANALYSES OF 14 PATIENTS WITH THE PRADER-WILLI SYNDROME AND OF 5 SUSPECTED INFANTS
    FUKUSHIMA, Y
    NIIKAWA, N
    KUROKI, Y
    JAPANESE JOURNAL OF HUMAN GENETICS, 1984, 29 (01): : 1 - 6
  • [46] THE PRADER-WILLI SYNDROME - A NEW CHROMOSOMAL DELETION SYNDROME
    SHEFFIELD, LJ
    FORD, JH
    WHITE, DI
    AUSTRALIAN PAEDIATRIC JOURNAL, 1982, 18 (02): : 154 - 154
  • [47] Genetic Studies of Prader-Willi Patients Provide Evidence for Conservation of Genomic Architecture in Proximal Chromosome 15q
    Hou, Aihua
    Lin, Shuan-Pei
    Ho, Shi Yun
    Chen, Chi-Fung Jennifer
    Lin, Hsiang-Yu
    Chen, Yen-Juin
    Huang, Chi-Yu
    Chiu, Huei-Ching
    Chuang, Chih-Kuang
    Chen, Ken-Shiung
    ANNALS OF HUMAN GENETICS, 2011, 75 : 211 - 221
  • [48] An unusual translocation within the Prader-Willi/Angelman syndrome critical region in 15q11-15q13 associated with clinical Prader-Willi syndrome.
    Schwartz, S
    Grebe, T
    Wolff, D
    Becker, L
    Conroy, J
    Nicholls, RD
    Horsthemke, B
    Buiting, K
    Cassidy, SB
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 64 (04): : 3 - 3
  • [49] Neural correlates of task switching in paternal 15q11-q13 deletion Prader-Willi syndrome
    Woodcock, Kate A.
    Humphreys, Glyn W.
    Oliver, Chris
    Hansen, Peter C.
    BRAIN RESEARCH, 2010, 1363 : 128 - 142
  • [50] PRADER-WILLI OR ANGELMAN SYNDROME IN FAMILIAL 15Q11-]Q13 DELETION OF MATERNAL ORIGIN
    SCHINZEL, A
    ROBINSON, WP
    BOTTANI, A
    XIE, YG
    PRADER, A
    HUMAN GENETICS, 1992, 88 (03) : 361 - 362
12345