DELETION (15Q) AS A CAUSE OF THE PRADER-WILLI SYNDROME (PWS)

被引:0
|
作者
LEDBETTER, DH
RICCARDI, VM
YOUNGBLOOM, SA
STROBEL, RJ
KEENAN, BS
CRAWFORD, JD
LOURO, JM
机构
[1] BAYLOR COLL MED, HOUSTON, TX 77030 USA
[2] MASSACHUSETTS GEN HOSP, BOSTON, MA 02114 USA
[3] UNIV TEXAS SAN ANTONIO, SAN ANTONIO, TX 78285 USA
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:A77 / A77
页数:1
相关论文
共 50 条
  • [1] DUPLICATION OF PROXIMAL 15Q AS A CAUSE OF PRADER-WILLI SYNDROME
    PETTIGREW, AL
    GOLLIN, SM
    GREENBERG, F
    RICCARDI, VM
    LEDBETTER, DH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (04): : 791 - 802
  • [2] PROBLEMS IN THE DETECTION OF 15Q DELETION IN PATIENTS WITH PRADER-WILLI SYNDROME
    WYANDT, HE
    PATIL, S
    SHAH, HO
    HANSON, JW
    ZELLWEGER, H
    KELLY, TE
    DOLAN, LM
    WILSON, WG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1981, 33 (06) : A127 - A127
  • [3] EXPANDED PRADER-WILLI SYNDROME IN A BOY WITH AN UNUSUAL 15Q CHROMOSOME DELETION
    PAULI, RM
    MEISNER, LF
    SZMANDA, RJ
    AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1983, 137 (11): : 1087 - 1089
  • [4] Unique maternal deletion of 15q in a patient with some symptoms of Prader-Willi syndrome
    Ninomiya, S
    Yokoyama, Y
    Kawakami, M
    Une, T
    Maruyama, H
    Morishima, T
    PEDIATRICS INTERNATIONAL, 2005, 47 (05) : 541 - 545
  • [5] DELETIONS OF PROXIMAL 15Q WITHOUT PRADER-WILLI SYNDROME
    GREENBERG, F
    LEDBETTER, DH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (04): : 813 - 820
  • [6] DELETION OF THE PARACENTROMERIC REGION OF 15Q11.2 IN A CASE OF PRADER-WILLI SYNDROME WITH T(15Q - 15Q) AND MARKER CHROMOSOME
    HIRAMOTO, K
    NARAHARA, K
    MURAO, S
    MIYAKE, S
    TAKAHASHI, Y
    WAKITA, Y
    KIKKAWA, K
    KIMURA, S
    KIMOTO, H
    TERATOLOGY, 1986, 34 (03) : 481 - 481
  • [7] Mosaicism of proximal 15q duplication/deletion resulting in Prader-Willi syndrome with normal methylation
    Boyd, L
    Brown, MG
    Kelson, S
    Lawce, H
    Shuttleworth, S
    Unsworth, N
    Magenis, RE
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 138A (02) : 181 - 184
  • [8] Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15
    Cassidy, SB
    Forsythe, M
    Heeger, S
    Nicholls, RD
    Schork, N
    Benn, P
    Schwartz, S
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 68 (04): : 433 - 440
  • [9] Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15)
    Varela, MC
    Lopes, GMP
    Koiffmann, CP
    ANNALES DE GENETIQUE, 2004, 47 (03): : 267 - 273
  • [10] 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