Prenatal diagnosis of a de novo triplication of chromosome 9p:46,XY,trp(9)(9pter→p13::p13→p24::p24→qter)

被引：0
|
作者：
Smith, G
Stewart, FJ
Thornton, CT
Brown, A
机构：
[1] Belfast City Hosp, Reg Genet Ctr, Belfast BT9 7AB, Antrim, North Ireland
[2] Royal Grp Hosp Trust, Dept Pathol, Belfast BT12 6BA, Antrim, North Ireland
[3] Southmead Gen Hosp, Dept Clin Chem, Lewis Lab, Dept Biochem Unit, Bristol BS10 5NB, Avon, England
来源：
JOURNAL OF MEDICAL GENETICS | 2000年 / 37卷
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：
208
引用
收藏
页码：S46 / S46
页数：1
相关论文
共 50 条
  • [1] 4 CASES OF CHROMOSOMAL DUPLICATION - 2 TANDEM DUPLICATIONS 9 (P24-]P13) AND 11(P14-]P13) AND TWO INVERTED TANDEM DUPLICATIONS 9(P24-]P13) AND 12(P13-]P12.2)
    BACCICHETTI, C
    ARTIFONI, L
    LENZINI, E
    PIOVAN, E
    CLINICAL GENETICS, 1981, 19 (06) : 489 - 490
  • [2] Direct duplication of 9p22→p24 in a child with duplication 9p syndrome
    Fujimoto, A
    Lin, MS
    Schwartz, S
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1998, 77 (04): : 268 - 271
  • [3] A 9p13→p24 duplication coupled with a whole 22q translocation onto 9p24
    Rivera, Horacio
    Vasquez-Velasquez, Ana I.
    de Lourdes Ramirez-Duenas, Maria
    Becerra-Solano, Luis Eduardo
    JOURNAL OF APPLIED GENETICS, 2007, 48 (01) : 95 - 98
  • [4] A 9p13→p24 duplication coupled with a whole 22q translocation onto 9p24
    Horacio Rivera
    Ana I. Vásquez-Velásquez
    María de Lourdes Ramírez-Dueńas
    Luis Eduardo Becerra-Solano
    Journal of Applied Genetics, 2007, 48 : 95 - 98
  • [5] NOR ACTIVITY AND CENTROMERE SUPPRESSION RELATED IN A DE-NOVO FUSION TDIC(9,13)(P22,P13) CHROMOSOME IN A CHILD WITH DEL(9P) SYNDROME
    DANIEL, A
    EKBLOM, L
    PHILLIPS, S
    FITZGERALD, JM
    OPITZ, JM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 22 (03): : 577 - 584
  • [6] Partial 9p monosomy in a child with a der(9)t(9;11)(p24;p15.4) identified by chromosome microdissection.
    Wattendorf, C
    Krasnewich, D
    Smith, A
    Meck, J
    Trent, J
    Dennis, T
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 332 - 332
  • [7] Prenatal diagnosis of del(9)(p24): a sex reverse case
    Privitera, O
    Vessecchia, G
    Bernasconi, B
    Bettio, D
    Stioui, S
    Giordano, G
    PRENATAL DIAGNOSIS, 2005, 25 (10) : 945 - 948
  • [8] Prenatal Diagnosis of a Female Fetus with Ring Chromosome 9, 46,XX, r(9)(p24q34), and a de novo Interstitial 9p Deletion
    Penacho, Vanessa
    Galan, Francisco
    Martin-Bayon, Tina-A.
    Mayo, Sonia
    Manchon, Irene
    Carrasco, Alfonso
    Martinez-Castellano, Francisco
    Alcaraz, Luis A.
    CYTOGENETIC AND GENOME RESEARCH, 2014, 144 (04) : 275 - 279
  • [9] Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22
    Verheij, JBGM
    Bouman, K
    van Lingen, RA
    Campagne, JGV
    Leegte, B
    van der Veen, AY
    Hofstra, RMW
    Buys, CHCM
    van Essen, AJ
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 86 (02): : 168 - 173
  • [10] ASSIGNMENT OF THE GENE FOR CD9 (P24) ANTIGEN TO 12P13
    VANCONG, N
    BENOIT, P
    GROSS, MS
    UZAN, G
    FRACHET, P
    MARGUERIE, G
    FREZAL, J
    BOUCHEIX, C
    CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 1096 - 1096
12345