PARENTAL ORIGIN OF THE EXTRA CHROMOSOME IN THE CAT EYE SYNDROME - EVIDENCE FROM HETEROMORPHISM AND INSITU HYBRIDIZATION ANALYSIS

被引:22
作者
MAGENIS, RE
SHEEHY, RR
BROWN, MG
MCDERMID, HE
WHITE, BN
ZONANA, J
WELEBER, R
机构
[1] OREGON HLTH SCI UNIV, CTR CHILD DEV REHAB, DIV CRIPPLED CHILDRENS, PORTLAND, OR 97201 USA
[2] OREGON HLTH SCI UNIV, CTR CHILD DEV REHAB, DEPT OPHTHALMOL, PORTLAND, OR 97201 USA
[3] OREGON HLTH SCI UNIV, CTR CHILD DEV REHAB, UNIV HOSP, CLIN CYTOGENET LAB, PORTLAND, OR 97201 USA
[4] QUEENS UNIV, DEPT BIOL, KINGSTON K7L 3N6, ONTARIO, CANADA
[5] CHILDRENS HOSP, PHILADELPHIA, PA 19104 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 29卷 / 01期
关键词
D O I
10.1002/ajmg.1320290103
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:9 / 19
页数:11
相关论文
共 32 条
[1]   LOCALIZATION OF HETEROCHROMATIN IN HUMAN CHROMOSOMES [J].
ARRIGHI, FE ;
HSU, TC .
CYTOGENETICS, 1971, 10 (02) :81-&
[2]   CAT-EYE SYNDROME - PARTIAL TRISOMY 22 [J].
BUHLER, EM ;
STALDER, GR ;
MEHES, K ;
MULLER, H .
HUMANGENETIK, 1972, 15 (02) :150-&
[3]   CLINICAL AND CYTOGENETIC SURVEY OF 39 INDIVIDUALS WITH PRADER-LABHART-WILLI SYNDROME [J].
BUTLER, MG ;
MEANEY, FJ ;
PALMER, CG .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) :793-809
[4]  
CASPERSSON T, 1970, CHROMOSOMA, V30, P215
[5]   A DELETION IN CHROMOSOME-22 CAN CAUSE DIGEORGE SYNDROME [J].
DELACHAPELLE, A ;
HERVA, R ;
KOIVISTO, M ;
AULA, P .
HUMAN GENETICS, 1981, 57 (03) :253-256
[6]   ISOLATION OF MOLECULAR PROBES ASSOCIATED WITH THE CHROMOSOME-15 INSTABILITY IN THE PRADER-WILLI SYNDROME [J].
DONLON, TA ;
LALANDE, M ;
WYMAN, A ;
BRUNS, G ;
LATT, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (12) :4408-4412
[7]  
DUNCAN AMV, 1986, AM J HUM GENET, V38, P978
[8]   THE 11Q-22Q TRANSLOCATION - A EUROPEAN COLLABORATIVE ANALYSIS OF 43 CASES [J].
FRACCARO, M ;
LINDSTEN, J ;
FORD, CE ;
ISELIUS, L ;
ANTONELLI, A ;
AULA, P ;
AURIAS, A ;
BAIN, AD ;
BARTSCHSANDHOFF, M ;
BERNARDI, F ;
BOYD, E ;
BUCHANAN, LF ;
CAMERON, AH ;
DELACHAPELLE, A ;
CIUFFA, G ;
CUOCO, C ;
DUTRILLAUX, B ;
DUTTON, G ;
FERGUSONSMITH, MA ;
FRANCESCONI, D ;
GERAEDTS, JPM ;
GIMELLI, G ;
GUEGUEN, J ;
GARSNER, E ;
HAGEMEIJER, A ;
HANSEN, FJ ;
HOLLINGS, PE ;
HUSTINX, TWJ ;
KAAKINEN, A ;
VANDEKAMP, JJP ;
KOSKULL, HV ;
LEJEUNE, J ;
LINDENBAUM, RH ;
MCCREANOR, HR ;
MIKKELSEN, M ;
MITELMAN, F ;
NICOLETTI, B ;
NILSBY, I ;
NILSSON, A ;
NOEL, B ;
PADOVANI, E ;
PASQUALI, F ;
PATER, JD ;
PEDERSEN, C ;
PETERSEN, F ;
ROBSON, EB ;
ROTMAN, J ;
RYYNANEN, M ;
SACHS, E ;
SALAT, J .
HUMAN GENETICS, 1980, 56 (01) :21-51
[9]   QUANTITATIVE-ANALYSIS OF HIGH-RESOLUTION TRYPSIN-GIEMSA BANDS ON HUMAN PROMETAPHASE CHROMOSOMES [J].
FRANCKE, U ;
OLIVER, N .
HUMAN GENETICS, 1978, 45 (02) :137-165
[10]  
GABARRON J, 1985, CLIN GENET, V28, P509