DELETIONS OF GENES AND ANONYMOUS DNA PROBES IN 2 BOYS WITH GREIG CEPHALOPOLYSYNDACTYLY SYNDROME

被引:0
|
作者
WAGNER, K
KROISEL, PM
ROSENKRANZ, W
机构
[1] INST MED BIOL & HUMAN GENET,A-8010 GRAZ,AUSTRIA
[2] UNIV MIAMI,SCH MED,DEPT BIOCHEM & MOLEC BIOL,MIAMI,FL 33136
来源
CYTOGENETICS AND CELL GENETICS | 1991年 / 58卷 / 3-4期
关键词
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
引用
下载
收藏
页码:1926 / 1927
页数:2
相关论文
共 44 条
  • [1] Molecular analysis of Greig cephalopolysyndactyly syndrome shows a high frequency of deletions.
    Olivos-Glander, IM
    Blancato, J
    Meck, J
    Biesecker, LG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A483 - A483
  • [2] GLI3 deletions associated with Greig cephalopolysyndactyly and implications for phenotypic overlap with Acrocallosal syndrome.
    Olivos-Glander, IM
    Blancato, J
    Meck, J
    Biesecker, LG
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 14 - 14
  • [3] Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3
    Jane A Hurst
    Dagan Jenkins
    Pradeep C Vasudevan
    Maria Kirchhoff
    Flemming Skovby
    Claudine Rieubland
    Sabina Gallati
    Olaf Rittinger
    Peter M Kroisel
    David Johnson
    Leslie G Biesecker
    Andrew OM Wilkie
    European Journal of Human Genetics, 2011, 19 : 757 - 762
  • [4] Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3
    Hurst, Jane A.
    Jenkins, Dagan
    Vasudevan, Pradeep C.
    Kirchhoff, Maria
    Skovby, Flemming
    Rieubland, Claudine
    Gallati, Sabina
    Rittinger, Olaf
    Kroisel, Peter M.
    Johnson, David
    Biesecker, Leslie G.
    Wilkie, Andrew O. M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (07) : 757 - 762
  • [5] MODY type 2 in Greig Cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome
    Zung, Amnon
    Ben-Yehoshua, Sagi Josefsberg
    HORMONE RESEARCH, 2008, 70 : 52 - 52
  • [6] MODY Type 2 in Greig Cephalopolysyndactyly Syndrome (GCPS) as Part of a Contiguous Gene Deletion Syndrome
    Zung, Amnon
    Petek, Erwin
    Ben-Zeev, Bruria
    Schwarzbraun, Thomas
    Ben-Yehoshua, Sagi Josefsberg
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (10) : 2469 - 2472
  • [7] THE USE OF CDNA PROBES FOR DETECTION OF DELETIONS IN DNA OF DUCHENNE MUSCULAR-DYSTROPHY BOYS
    POPOWSKA, E
    POPOWSKI, J
    KRAJEWSKAWALASEK, M
    PRONICKA, E
    PEDIATRIC RESEARCH, 1989, 26 (05) : 515 - 515
  • [8] DELETION OF EGFR-GENE IN ONE OF 2 PATIENTS WITH GREIG CEPHALOPOLYSYNDACTYLY SYNDROME AND MICRODELETION OF CHROMOSOME-7P
    ROSENKRANZ, W
    KROISEL, PM
    WAGNER, K
    CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 1069 - 1069
  • [9] LOCALIZATION OF GENES AND ANONYMOUS DNA PROBES ON THE SHORT ARM OF CHROMOSOME-7
    WAGNER, K
    KROISEL, PM
    ROSENKRANZ, W
    MAMMALIAN GENOME, 1992, 3 (01) : 39 - 41
  • [10] CHARACTERIZATION OF CHROMOSOME-7 LONG ARM DELETIONS BY DNA PROBES IN MYELODYSPLASTIC SYNDROME
    KERE, J
    RUUTU, T
    DELACHAPELLE, A
    EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1987, 23 (11): : 1767 - 1767