Gingival fibromatosis and partial duplication of the short arm of chromosome 2 (dup(2)(p13->p21)).

被引：0
|
作者：
Fryns, JP
机构：
来源：
ANNALES DE GENETIQUE | 1996年 / 39卷 / 01期
关键词：
chromosome; 2; gingival fibromatosis; mental retardation;
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
Gingival fibromatosis and partial duplication of the short arm of chromosome 2 (dup(2)(p13--> p21)).
引用
收藏
页码：54 / 55
页数：2
相关论文
共 34 条
  • [21] PORTOHEPATIC SHUNT IN A DOWN-SYNDROME PATIENT WITH AN INTERCHANGE TRISOMY 47,XY,-2,+DER(2),+DER(21)T(2 21)(P13 Q22.1)MAT
    KIERAN, MW
    VEKEMANS, M
    ROBB, LJ
    SINSKY, A
    OUTERBRIDGE, EW
    DERKALOUSTIAN, VM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (03): : 288 - 292
  • [22] Prenatal detection of de novo inversion of chromosome (2) (p13q11.2) and postnatal follow-up
    Kozma, C
    Subasinghe, C
    Meck, J
    PRENATAL DIAGNOSIS, 1996, 16 (04) : 366 - 370
  • [23] The human dihydropyrimidinase-related protein 2 gene on chromosome 8p21 is associated with paranoid-type schizophrenia
    Nakata, K
    Ujike, H
    Sakai, A
    Takaki, M
    Imamura, T
    Tanaka, Y
    Kuroda, S
    BIOLOGICAL PSYCHIATRY, 2003, 53 (07) : 571 - 576
  • [24] High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers
    Eiriksdottir, G
    Barkardottir, RB
    Agnarsson, BA
    Johannesdottir, G
    Olafsdottir, K
    Egilsson, V
    Ingvarsson, S
    ONCOGENE, 1998, 16 (01) : 21 - 26
  • [25] An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion
    Lybaek, Helle
    Orstavik, Karen Helene
    Prescott, Trine
    Hovland, Randi
    Breilid, Harald
    Stansberg, Christine
    Steen, Vidar Martin
    Houge, Gunnar
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2009, 17 (07) : 904 - 910
  • [26] Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.19, 6q26-q27, and 21q2
    Dobyns, William B.
    Mirzaa, Ghayda
    Christian, Susan L.
    Petras, Kristin
    Roseberry, Jessica
    Clark, Gary D.
    Curry, Cynthia J. R.
    McDonald-McGinn, Donna
    Medne, Livija
    Zackai, Elaine
    Parsons, Julie
    Zand, Dina J.
    Hisama, Fuki M.
    Walsh, Christopher A.
    Leventer, Richard J.
    Martin, Christa L.
    Gajecka, Marzena
    Shaffer, Lisa G.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (13) : 1637 - 1654
  • [27] Concomitant deletion of the short arm (Del 1p13.3) and amplification or gain (1q21) of chromosome 1 by fluorescence in situ hybridization are associated with a poor clinical outcome in multiple myeloma
    Mohan, Meera
    Gong, Zimu
    Ashby, Timothy Cody
    Al Hadidi, Samer
    Thanendrarajan, Sharmilan
    Schinke, Carolina
    Alapat, Daisy
    Shaughnessy Jr, John D. D.
    Zhan, Fenghuang
    van Rhee, Frits
    Sawyer, Jeffery R.
    Tian, Erming
    Zangari, Maurizio
    CANCER, 2023, 129 (16) : 2491 - 2498
  • [28] Association between genetic variants at chromosome 9p21 and risk of coronary artery disease in Emirati Type 2 Diabetes patients
    Baalfaqih, Zahrah
    Sulaiman, Fatima
    Abu-Samra, Nadia
    Alshaikh, Manar
    Mawart, Aurelie
    Osman, Wael
    Al Mahmeed, Wael
    Tay, Guan
    Alsafar, Habiba
    GENE REPORTS, 2020, 21
  • [29] Microsatellite marker association at chromosome region 2p13 in Finnish patients with preeclampsia and obstetric cholestasis suggests a common risk locus
    Laasanen, J
    Hiltunen, M
    Romppanen, EL
    Punnonen, K
    Mannermaa, A
    Heinonen, S
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2003, 11 (03) : 232 - 236
  • [30] A new case of 2q duplication supports either a locus for orofacial clefting between markers D2S1897 and D2S2023 or a locus for cleft palate only on chromosome 2q13-q21
    Ounap, K
    Ilus, T
    Laidre, P
    Uibo, O
    Tammur, P
    Bartsch, O
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 137A (03) : 323 - 327
1234