DUPLICATION 3Q SYNDROME - MOLECULAR DELINEATION OF THE CRITICAL REGION

被引:66
作者
AQUA, MS
RIZZU, P
LINDSAY, EA
SHAFFER, LG
ZACKAI, EH
OVERHAUSER, J
BALDINI, A
机构
[1] BAYLOR COLL MED,DEPT MOLEC & HUMAN GENET,HOUSTON,TX 77030
[2] BAYLOR COLL MED,CTR HUMAN GENOME,HOUSTON,TX
[3] CHILDRENS HOSP,DEPT GENET,PHILADELPHIA,PA 19104
[4] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT BIOCHEM & MOLEC BIOL,PHILADELPHIA,PA 19107
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 55卷 / 01期
关键词
DUP(3) SYNDROME; MOLECULAR ANALYSIS; CRITICAL REGION;
D O I
10.1002/ajmg.1320550111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The phenotype of dup(3q) syndrome partially overlaps with Brachmann-de Lange phenotype, Convulsions and eye, palate renal, and cardiac anomalies are more frequent in dup(3q) syndrome, while limb deficiencies, hirsutism, and synophrys are more characteristic of Brachmann-de Lange syndrome, Whether the two syndromes have a biological relationship has yet to be demonstrated, Using two patient translocation cell lines, each involving distal 3q, we have narrowed the critical region of the dup(3q) syndrome to the interval 3q26,31-q27,3 and initiated its molecular characterization. We have mapped in this region 6 cosmid clones spanning approximately 3-5 Mb, The critical region appears to overlap with the region where a balanced translocation was found in a Brachmann-de Lange patient, This work provides the mapping framework for finer molecular analysis of dup(3q) syndrome. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:33 / 37
页数:5
相关论文
共 25 条
  • [1] ALLDERDICE PW, 1975, AM J HUM GENET, V27, P699
  • [2] CHROMOSOMAL ASSIGNMENT OF HUMAN YAC CLONES BY FLUORESCENCE INSITU HYBRIDIZATION - USE OF SINGLE-YEAST-COLONY PCR AND MULTIPLE LABELING
    BALDINI, A
    ROSS, M
    NIZETIC, D
    VATCHEVA, R
    LINDSAY, EA
    LEHRACH, H
    SINISCALCO, M
    [J]. GENOMICS, 1992, 14 (01) : 181 - 184
  • [3] FALEK A, 1966, PEDIATRICS, V37, P92
  • [4] FINEMAN RM, 1978, PEDIATRICS, V61, P611
  • [5] CHROMOSOME 3Q DUPLICATION AND THE BRACHMANN-DELANGE SYNDROME (BDLS)
    FRANCKE, U
    OPITZ, JM
    [J]. JOURNAL OF PEDIATRICS, 1979, 95 (01) : 161 - 162
  • [6] A DENOVO TRANSLOCATION T(3-17)(Q26.3-Q23.1) IN A CHILD WITH CORNELIA-DE-LANGE-SYNDROME
    IRELAND, M
    ENGLISH, C
    CROSS, I
    HOULSBY, WT
    BURN, J
    [J]. JOURNAL OF MEDICAL GENETICS, 1991, 28 (09) : 639 - 640
  • [7] INTERPHASE AND METAPHASE RESOLUTION OF DIFFERENT DISTANCES WITHIN THE HUMAN DYSTROPHIN GENE
    LAWRENCE, JB
    SINGER, RH
    MCNEIL, JA
    [J]. SCIENCE, 1990, 249 (4971) : 928 - 932
  • [8] PARTIAL DUPLICATION OF 3Q (Q25.1-]Q26.1) WITHOUT THE BRACHMANN-DELANGE PHENOTYPE
    LOPEZRANGEL, E
    DILL, FJ
    HRYNCHAK, MA
    VANALLEN, MI
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (07): : 1068 - 1071
  • [9] DUP 3(Q) SYNDROME AND NEUROBLASTOMA
    MAIER, B
    BECK, JD
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1992, 151 (09) : 715 - 716
  • [10] McKusick VA, 1992, MENDELIAN INHERITANC