Cytogenetic, molecular and sequence analyses of neocentromeric sequences from 9p: implications for activation of neocentromeres.

被引：0
|
作者：
Satinover, DL [1 ]
Schwartz, S [1 ]
机构：
[1] Case Western Reserve Univ, Univ Hosp Cleveland, Dept Genet, Cleveland, OH USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67卷 / 04期
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：
168
引用
收藏
页码：44 / 44
页数：1
相关论文
共 35 条
  • [21] Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication
    Yueh-Chun Li
    Yi-Ju Pan
    Fuu-Jen Tsai
    Chyi-Chyang Lin
    Genes & Genomics, 2016, 38 : 53 - 57
  • [22] Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication
    Li, Yueh-Chun
    Pan, Yi-Ju
    Tsai, Fuu-Jen
    Lin, Chyi-Chyang
    GENES & GENOMICS, 2016, 38 (01) : 53 - 57
  • [23] Pseudoplatystoma metaense and P. orinocoense (Siluriformes: Pimelodidae) from the Orinoco basin, Venezuela: cytogenetic and molecular analyses
    Nirchio, M.
    Mujica, A.
    Oliveira, C.
    Granado, A.
    Mora, J.
    Hett, A. K.
    Rossi, A. R.
    Milana, V.
    Sola, L.
    ITALIAN JOURNAL OF ZOOLOGY, 2013, 80 (04) : 526 - 535
  • [24] 4 CASES OF 9P TRISOMY RESULTING FROM A BALANCED FAMILIAL TRANSLOCATION (9-15) (Q13-Q11) - CLINICAL PICTURE AND CYTOGENETIC FINDINGS
    ZAREMBA, J
    ZDZIENICKA, E
    GLOGOWSKA, I
    ABRAMOWICZ, T
    TARACHA, B
    JOURNAL OF MENTAL DEFICIENCY RESEARCH, 1974, 18 (JUN): : 153 - 190
  • [25] MOLECULAR DEFINITION OF A CHROMOSOME-9P21 GERM-LINE DELETION IN A WOMAN WITH MULTIPLE MELANOMAS AND A PLEXIFORM NEUROFIBROMA - IMPLICATIONS FOR 9P TUMOR-SUPPRESSOR GENE(S)
    PETTY, EM
    GIBSON, LH
    FOUNTAIN, JW
    BOLOGNIA, JL
    YANGFENG, TL
    HOUSMAN, DE
    BALE, AE
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (01) : 96 - 104
  • [26] Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9) t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication
    Chen, Chih-Ping
    Lin, Chen-Ju
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Yen-Ni
    Chen, Shin-Wen
    Lee, Chen-Chi
    Chen, Li-Feng
    Yang, Chien-Wen
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (04): : 596 - 601
  • [27] Gain of chromosome arm 9p is characteristic of primary mediastinal B-cell lymphoma (MBL):: Comprehensive molecular cytogenetic analysis and presentation of a novel MBL cell line
    Bentz, M
    Barth, TFE
    Brüderlein, S
    Bock, D
    Schwerer, MJ
    Baudis, M
    Joos, S
    Viardot, A
    Feller, AC
    Müller-Hermelink, HK
    Lichter, P
    Döhner, H
    Möller, P
    GENES CHROMOSOMES & CANCER, 2001, 30 (04): : 393 - 401
  • [28] Phenotypic and cytogenetic analysis of a liveborn infant with prenatally detected trisomy 9p and partial trisomy 8p resulting from 3:1 malsegregation of a maternal reciprocal translocation.
    Smith, R
    Wyandt, HE
    Milunsky, JM
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 334 - 334
  • [29] Phenotypic and molecular characterization of partial 2q trisomy and partial 9p monosomy resulting from a maternal balanced translocation. A case report
    Bastida, N.
    Crettaz, J.
    Muguerza, R.
    Marti, I.
    Martinez-Mugica, O.
    Ramirez, Y.
    Otaolea, L.
    Saez, R.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 509 - 509
  • [30] SEQUENCE EVOLUTION IN MITOCHONDRIAL RIBOSOMAL AND ND-1 GENES IN LEPIDOPTERA - IMPLICATIONS FOR PHYLOGENETIC ANALYSES (MOLECULAR-BIOLOGY AND EVOLUTION, VOL 9, PG 1061, 1992)
    PASHLEY
    KE
    MOLECULAR BIOLOGY AND EVOLUTION, 1993, 10 (01) : 268 - 268
1234