CONFERENCE REPORT - 1ST INTERNATIONAL SCIENTIFIC WORKSHOP ON PRADER-WILLI SYNDROME AND OTHER CHROMOSOME 15Q DELETION DISORDERS

被引:7
|
作者
CASSIDY, SB [1 ]
机构
[1] UNIV ARIZONA,COLL MED,STEELE MEM CHILDRENS RES CTR,TUCSON,AZ 85724
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 42卷 / 02期
关键词
PRADER-WILLI SYNDROME; ANGELMAN SYNDROME; CHROMOSOME DELETION; 15Q DELETION; GENETIC IMPRINTING; DISOMY; CONTIGUOUS GENE SYNDROME; GROWTH HORMONE; SLEEP DISORDER; DIAGNOSTIC CRITERIA;
D O I
10.1002/ajmg.1320420221
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:220 / 230
页数:11
相关论文
共 50 条
  • [31] CONFERENCE REPORT - 2ND ANNUAL PRADER-WILLI SYNDROME SCIENTIFIC CONFERENCE
    LEDBETTER, DH
    GREENBERG, F
    HOLM, VA
    CASSIDY, SB
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (04): : 779 - 790
  • [32] 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
  • [33] Detection of chromosome 15 deletion in Prader-Willi syndrome using fluorescence in situ hybridization
    Suzuki, Y
    Sasagawa, I
    Yazawa, H
    Tateno, T
    Nakada, T
    ARCHIVES OF ANDROLOGY, 2000, 45 (01): : 13 - 17
  • [34] Prader-Willi syndrome:: A case report of a Hispanic patient with a 15:20 translocation and deletion of 15q13.
    Wall, JB
    Viskochil, D
    JOURNAL OF INVESTIGATIVE MEDICINE, 1998, 46 (01) : 120A - 120A
  • [35] FAMILIAL PRADER-WILLI SYNDROME WITH PRECOCIOUS PUBERTY AND NORMAL CHROMOSOME-15Q
    CLERICUZIO, CL
    ROSE, SR
    LAI, LW
    CASSIDY, SB
    CLINICAL RESEARCH, 1993, 41 (01): : A71 - A71
  • [36] 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
  • [37] 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
  • [38] 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
  • [39] OCCUPATIONAL HYDROCARBON EXPOSURE AMONG FATHERS OF PRADER-WILLI SYNDROME PATIENTS WITH AND WITHOUT DELETIONS OF 15Q
    CASSIDY, SB
    GAINEY, AJ
    BUTLER, MG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1989, 44 (06) : 806 - 810
  • [40] A case of an atypically large proximal 15q deletion as cause for Prader-Willi syndrome arising from a de novo unbalanced translocation
    Hickey, Scott E.
    Thrush, Devon Lamb
    Walters-Sen, Lauren
    Reshmi, Shalini C.
    Astbury, Caroline
    Gastier-Foster, Julie M.
    Atkin, Joan
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2013, 56 (09) : 510 - 514