Paternal triplication of 15q11-q13 in a hypotonic, developmentally delayed child without Prader-Willi or angelman syndrome

被引:0
|
作者
Cassidy, SB [1 ]
Conroy, J [1 ]
Becker, L [1 ]
Schwartz, S [1 ]
机构
[1] CASE WESTERN RESERVE UNIV,SCH MED,DEPT GENET,CLEVELAND,OH 44106
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 62卷 / 03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:4 / 4
页数:2
相关论文
共 50 条
  • [41] Incidence of 15q11q13 deletions in spermatozoa from Prader-Willi syndrome fathers
    Molina, O.
    Anton, E.
    Vidal, F.
    Blanco, J.
    CHROMOSOME RESEARCH, 2007, 15 : 71 - 72
  • [42] DELETIONS OF PROXIMAL 15Q WITHOUT PRADER-WILLI SYNDROME
    GREENBERG, F
    LEDBETTER, DH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (04): : 813 - 820
  • [43] De Novo Interstitial Duplication of 15q11.2-q13.1 With Complex Maternal Uniparental Trisomy for the 15q11-q13 Region in a Patient with Prader-Willi Syndrome
    Burrage, Lindsay C.
    Person, Richard E.
    Flores, Angela
    Villanos, Maria Theresa M.
    Bi, Weimin
    Wiszniewska, Joanna
    Bacino, Carlos A.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (10) : 2557 - 2563
  • [44] Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13
    Eliez, S
    Morris, MA
    DahounHadorn, S
    DeLozierBlanchet, CD
    Gos, A
    Sizonenko, P
    Antonarakis, SE
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 70 (03): : 222 - 228
  • [45] PRADER-WILLI SYNDROME AND A 15Q-21Q TRANSLOCATION
    TETEAK, JE
    HENRY, J
    SANGER, WG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1983, 35 (06) : A156 - A156
  • [46] Mosaicism for del(15)(q11-q12) underlying the Prader-Willi syndrome
    Missirian, C
    Malzac, P
    Mattei, MG
    Voelckel, MA
    Mattei, JF
    Moncla, A
    EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 : 95 - 96
  • [47] Frequencies of de novo 15q11q13 inversions in spermatozoa of Prader-Willi syndrome fathers
    Molina, Oscar
    Anton, Ester
    Vidal, Francesca
    Blanco, Joan
    CHROMOSOME RESEARCH, 2011, 19 : S129 - S130
  • [48] IDENTIFICATION IMPRINTING GENE EXPRESSION AT 15Q11-Q13 REGION IN ANGELMAN SYNDROME
    Vijayakumar, P.
    PARKINSONISM & RELATED DISORDERS, 2018, 46 : E53 - E54
  • [49] PRADER-WILLI SYNDROME IN A BROTHER AND SISTER WITHOUT CYTOGENETIC OR DETECTABLE MOLECULAR GENETIC ABNORMALITY AT CHROMOSOME 15Q11Q13
    ORSTAVIK, KH
    TANGSRUD, SE
    KIIL, R
    HANSTEEN, IL
    STEENJOHNSEN, J
    CASSIDY, SB
    MARTONY, A
    ANVRET, M
    TOMMERUP, N
    BRONDUMNIELSEN, K
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (04): : 534 - 538
  • [50] PHYSICAL MAPPING AND ISOLATION OF EXPRESSED SEQUENCES IN THE PRADER-WILLI ANGELMAN CRITICAL REGION OF CHROMOSOME 15Q11-]Q13
    SUTCLIFFE, JS
    NAKAO, M
    MUTIRANGURA, A
    CHRISTIAN, S
    LEDBETTER, DH
    BEAUDET, AL
    CYTOGENETICS AND CELL GENETICS, 1994, 67 (01): : 19 - 19