Molecular analysis of 15q11-13 region in Prader-Willi and Angelman syndromes

被引：0
|
作者：
Bielinska, B [1 ]
Popowska, E [1 ]
Krajewska-Walasek, M [1 ]
机构：
[1] Childrens Mem Hlth Inst, Dept Med Genet, Warsaw, Poland
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 1998年 / 6卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P4102
引用
收藏
页码：134 / 134
页数：1
相关论文
共 50 条
  • [31] Prader-Willi and Angelman Syndromes: Mechanisms and Management
    Ma, Van K.
    Mao, Rong
    Toth, Jessica N.
    Fulmer, Makenzie L.
    Egense, Alena S.
    Shankar, Suma P.
    APPLICATION OF CLINICAL GENETICS, 2023, 16 : 41 - 52
  • [32] Diagnostic possibilities of Prader-Willi and of Angelman syndromes
    Calounová, G
    Bóday, A
    Havlovicová, M
    Zumrová, A
    Kocárek, E
    Novotná, D
    Maríková, T
    Apltová, L
    Stevove, J
    Goetz, P
    CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE, 2005, 68 (05) : 284 - 293
  • [33] DUPLICATION OF CHROMOSOME-15Q IN PRADER-WILLI AND ANGELMAN SYNDROMES - A GENE DOSAGE PARADOX
    MUTIRANGURA, A
    KUWANO, A
    ROBINSON, WP
    GREENBERG, F
    MALCOLM, S
    LEDBETTER, DH
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 584 - 584
  • [34] 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
  • [35] Prader-Willi and Angelman syndromes: genetic counseling
    Camprubi, Cristina
    Coll, Maria Dolors
    Gabau, Elisabeth
    Guitart, Miriam
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2010, 18 (02) : 154 - 155
  • [36] GENETIC TESTING FOR PRADER-WILLI AND ANGELMAN SYNDROMES
    SCHAD, CR
    JALAL, SM
    THIBODEAU, SN
    MAYO CLINIC PROCEEDINGS, 1995, 70 (12) : 1195 - 1196
  • [37] Origin of uniparental disomy 15 in Prader-Willi and Angelman syndromes.
    Fridman, C
    Koiffmann, CP
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A271 - A271
  • [38] An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder
    Curran, S
    Roberts, S
    Thomas, S
    Veltman, M
    Browne, J
    Medda, E
    Pickles, A
    Sham, P
    Bolton, PF
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2005, 137B (01) : 25 - 28
  • [39] Diagnostic testing: A cost analysis for Prader-Willi and Angelman syndromes
    Monaghan, KG
    VanDyke, DL
    Feldman, G
    Wiktor, A
    Weiss, L
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 60 (01) : 244 - 247
  • [40] DELETION OF 15Q11-]Q13 IN A MOTHER AND SON WITHOUT FEATURES OF PRADER-WILLI OR ANGELMAN SYNDROME
    PHELAN, MC
    MICHAELIS, RC
    TARLETON, JC
    DONLON, TA
    SKINNER, SA
    CYTOGENETICS AND CELL GENETICS, 1995, 69 (1-2): : 116 - 116
12345