MORPHOLOGY ALONE DOES NOT MAKE AN ISOCHROMOSOME

被引:7
作者
SCHMUTZ, SM [1 ]
PINNO, E [1 ]
机构
[1] REGINA GEN HOSP,CYTOGENET LAB,REGINA,SASKATCHEWAN,CANADA
关键词
D O I
10.1007/BF00291889
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:253 / 255
页数:3
相关论文
共 21 条
[1]   Misdivision and the genetics of the centromere [J].
Darlington, CD .
JOURNAL OF GENETICS, 1939, 37 (02) :341-U19
[2]   The origin of iso-chromosomes [J].
Darlington, CD .
JOURNAL OF GENETICS, 1940, 39 (02) :351-361
[3]   HOW DO HUMAN ISOCHROMOSOMES ARISE [J].
DELACHAPELLE, A .
CANCER GENETICS AND CYTOGENETICS, 1982, 5 (02) :173-179
[4]  
FROSTERISKENIUS U, 1984, CLIN GENET, V26, P549
[5]   TRISOMY-9P WITH I(9P) AND T(9Q18P) [J].
HERVA, R ;
KOIVISTO, M .
HUMAN GENETICS, 1979, 50 (03) :237-240
[6]   NUMBER OF C-BANDS OF HUMAN ISOCHROMOSOME XQI AND RELATION TO 45,X-MOSAICISM [J].
HSU, LYF ;
PACIUC, S ;
DAVID, K ;
CRISTIAN, S ;
MOLOSHOK, R ;
HIRSCHHORN, K .
JOURNAL OF MEDICAL GENETICS, 1978, 15 (03) :222-226
[7]   TRISOMY-18 SYNDROME WITH AN UNUSUAL KARYOTYPE - POSSIBLE DOUBLE ISOCHROMOSOME [J].
LARSON, LM ;
WASDAHL, WA ;
SAUMUR, JH ;
COLEMAN, ML ;
JALAL, SM .
JOURNAL OF MEDICAL GENETICS, 1978, 15 (01) :73-76
[8]   CHROMOSOME-15 ANOMALIES AND THE PRADER-WILLI SYNDROME - CYTOGENETIC ANALYSIS [J].
MATTEI, MG ;
SOUIAH, N ;
MATTEI, JF .
HUMAN GENETICS, 1984, 66 (04) :313-334
[9]  
MUELLER HE, 1972, J MED GENET, V9, P462
[10]  
NIKAWA N, 1983, HUM GENET, V63, P85