VALUE OF CHROMOSOME PAINTING IN DETERMINING THE CHROMOSOMAL OUTCOME IN OFFSPRING OF A 12/16 TRANSLOCATION CARRIER

被引:12
作者
BRANDT, CA
LYNGBYE, T
PEDERSEN, S
BOLUND, L
FRIEDRICH, U
机构
[1] AARHUS UNIV,INST HUMAN GENET,DK-8000 AARHUS,DENMARK
[2] AARHUS KOMMUNE HOSP,DEPT PAEDIAT,DK-8000 AARHUS,DENMARK
关键词
D O I
10.1136/jmg.31.3.234
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We currently use direct and reverse chromosome painting in prenatal diagnosis. In a family with a subtle 12;16 translocation, adjacent 1 segregation was diagnosed in the first child, a boy, in whom symptoms compatible with partial trisomy 16p and partial monosomy 12q were seen. In the next pregnancy, a chorionic villus biopsy was tested using chromosome painting. Only by supplementing conventional cytogenetic methods with molecular cytogenetic techniques could the true karyotype be unequivocally determined. Reverse painting, using DOP-PCR amplified, flow sorted paternal derivative chromosomes as a DNA library to paint the chorionic villus cells, was especially informative.
引用
收藏
页码:234 / 237
页数:4
相关论文
共 11 条
[1]  
BRANDT CA, 1993, CLIN GENET, V44, P26
[2]   PSEUDODICENTRIC CHROMOSOME 18 DIAGNOSED BY CHROMOSOME PAINTING AND PRIMED IN-SITU LABELING (PRINS) [J].
BRANDT, CA ;
DJERNES, B ;
STROMKJAER, H ;
PETERSEN, MB ;
PEDERSEN, S ;
HINDKJAER, J ;
BRINCHIVERSEN, J ;
BRUUNPETERSEN, G .
JOURNAL OF MEDICAL GENETICS, 1994, 31 (02) :99-102
[3]  
HINDKJAER J, 1991, INT J BIOTECH, V12, P752
[4]  
JAUCH A, 1990, HUM GENET, V85, P145
[5]   TRISOMY-16P IN A LIVEBORN OFFSPRING DUE TO MATERNAL TRANSLOCATION T(16 21)(Q11 P11) AND REVIEW OF THE LITERATURE [J].
LEONARD, C ;
HURET, JL ;
IMBERT, MC ;
LEBOUC, Y ;
SELVA, J ;
BOULLEY, AM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (03) :621-625
[6]   A HIGHLY CONSERVED REPETITIVE DNA-SEQUENCE, (TTAGGG)N, PRESENT AT THE TELOMERES OF HUMAN-CHROMOSOMES [J].
MOYZIS, RK ;
BUCKINGHAM, JM ;
CRAM, LS ;
DANI, M ;
DEAVEN, LL ;
JONES, MD ;
MEYNE, J ;
RATLIFF, RL ;
WU, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6622-6626
[7]  
PARK VM, 1992, AM J HUM GENET, V50, P914
[8]  
PEDERSEN S, METHODS MOL BIOL IN, P99
[9]   FLUORESCENCE INSITU HYBRIDIZATION WITH HUMAN CHROMOSOME-SPECIFIC LIBRARIES - DETECTION OF TRISOMY-21 AND TRANSLOCATIONS OF CHROMOSOME-4 [J].
PINKEL, D ;
LANDEGENT, J ;
COLLINS, C ;
FUSCOE, J ;
SEGRAVES, R ;
LUCAS, J ;
GRAY, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9138-9142
[10]  
SPELEMAN F, 1992, CLIN GENET, V41, P169