Large inv dup(15) chromosome in two generations

被引：1
|
作者：
VanDerSmagt, JJ
Giltay, JC
DeNef, JJEM
Slabbers, GHPR
机构：
[1] SPAARNE HOSP,DEPT PAEDIAT,HAARLEM,NETHERLANDS
[2] CLIN GENET CTR,UTRECHT,NETHERLANDS
来源：
JOURNAL OF MEDICAL GENETICS | 1996年 / 33卷 / 03期
关键词：
D O I：
10.1136/jmg.33.3.261-a
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：261 / 262
页数：2
相关论文
共 50 条
  • [21] AN ANALYSIS OF THE PARENTAL AGE EFFECT FOR INV DUP (15)
    CONNOR, JM
    GILMORE, DH
    JOURNAL OF MEDICAL GENETICS, 1984, 21 (03) : 213 - 214
  • [22] MOLECULAR CYTOGENETIC ANALYSIS OF INV DUP(15) CHROMOSOMES
    LEANACOX, J
    JENKINS, L
    PALMER, C
    PLATTNER, R
    SHEPPARD, L
    FLEJTER, W
    ZACKOWSKI, J
    SHAPIRA, E
    SCHWARTZ, S
    CYTOGENETICS AND CELL GENETICS, 1993, 63 (04): : 255 - 255
  • [23] Mosaic supernumerary inv dup(15) chromosome with four copies of the P gene in a boy with pigmentary dysplasia
    Akahoshi, K
    Spritz, RA
    Fukai, K
    Mitsui, N
    Matsushima, K
    Ohashi, H
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 126A (03) : 290 - 292
  • [24] The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)
    Agatino Battaglia
    Orphanet Journal of Rare Diseases, 3
  • [25] The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)
    Battaglia, Agatino
    ORPHANET JOURNAL OF RARE DISEASES, 2008, 3 (1)
  • [26] Partial hexasomy of 15qII-qI3 in a child with two supernumerary inv dup (15) chromosomes
    Sarri, C
    Cyftodimou, J
    Laskari, H
    Grigoriadou, M
    Pandelia, E
    Petersen, MB
    CYTOGENETICS AND CELL GENETICS, 1999, 85 (1-2): : 164 - 164
  • [27] Maternal origin of inv dup(15) chromosomes in infantile autism
    Martinsson, T
    Johannesson, T
    Vujic, M
    Sjostedt, A
    Steffenburg, S
    Gillberg, C
    Wahlstrom, J
    EUROPEAN CHILD & ADOLESCENT PSYCHIATRY, 1996, 5 (04) : 185 - 192
  • [28] Paternal origin of a small, class I Inv dup(15)
    Dawson, AJ
    Mogk, R
    Rothenmund, H
    Bridge, PJ
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 107 (04): : 334 - 336
  • [29] Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15)chromosome
    Wang, YM
    Chuang, L
    Wang, BT
    Kuo, PL
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2004, 103 (12) : 943 - 947
  • [30] The syndrome of inv dup (15): Clinical, electroencephalographic, and imaging findings
    Buoni, S
    Sorrentino, L
    Farnetani, MA
    Pucci, L
    Fois, A
    JOURNAL OF CHILD NEUROLOGY, 2000, 15 (06) : 380 - 385
12345