QUANTITATIVE-ANALYSIS OF C-BANDS IN CHROMOSOME-1, CHROMOSOME-9, AND CHROMOSOME-16 OF BRAZILIAN INDIANS AND CAUCASOIDS

被引：0

作者：

ERDTMANN, B ^{[1
]}

SALZANO, FM ^{[1
]}

MATTEVI, MS ^{[1
]}

FLORES, RZ ^{[1
]}

机构：

[1] UNIV FED RIO GRANDE SUL,INST BIOCIENCIAS,DEPT GENET,PORTO ALEGRE 90000,RS,BRAZIL

来源：

HUMAN GENETICS | 1981年 / 57卷 / 01期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：58 / 63

页数：6

共 50 条

[31] CENTROMERIC FRAGILITY OF CHROMOSOME-1, CHROMOSOME-2, CHROMOSOME-9, CHROMOSOME-16 AND FRA(16Q23) IN A CANCER FAMILY
SHABTAI, F
LURIE, B
REISFELD, I
KLAR, D
HALBRECHT, I
CLINICAL GENETICS, 1985, 27 (03) : 336 - 337
[32] A RAPID METHOD FOR IDENTIFICATION OF CONSTITUTIVE HETEROCHROMATIN OF SECONDARY CONSTRICTION REGIONS OF HUMAN CHROMOSOME-1, CHROMOSOME-9, AND CHROMOSOME-16
VERMA, RS
BRAT, SV
DOSIK, H
JOURNAL OF HEREDITY, 1982, 73 (01) : 74 - 76
[33] MITOMYCIN-C INDUCED STRUCTURAL-CHANGES IN HETEROCHROMATIC REGIONS OF HUMAN CHROMOSOME-1, CHROMOSOME-9, CHROMOSOME-16 AND CHROMOSOME-Y
MALYGINA, NA
REMIZOVA, OG
AKIFIEV, AP
TSITOLOGIYA, 1988, 30 (11): : 1350 - &
[34] CENTROMERIC INSTABILITY OF CHROMOSOME-1, CHROMOSOME-9 AND CHROMOSOME-16 WITH VARIABLE IMMUNE-DEFICIENCY - SUPPORT OF A NEW SYNDROME
VALKOVA, G
GHENEV, E
TZANCHEVA, M
CLINICAL GENETICS, 1987, 31 (03) : 119 - 124
[35] THE QUANTITATIVE-ANALYSIS OF POLYMORPHISM ON HUMAN CHROMOSOMES-1, CHROMOSOME-9, CHROMOSOME-16, AND CHROMOSOME-Y .4. HETEROGENEITY OF A NORMAL POPULATION
PODUGOLNIKOVA, OA
KOROSTELEV, AP
HUMAN GENETICS, 1980, 54 (02) : 163 - 169
[36] HETEROCHROMATIC REGIONS OF CHROMOSOME-1, CHROMOSOME-9, CHROMOSOME-16 AND CHROMOSOME-Y IN CHILDREN WITH SOME DISTURBANCES OCCURRING DURING THE EMBRYO DEVELOPMENT
PODUGOLNIKOVA, OA
BLYUMINA, MG
GENETIKA, 1982, 18 (12): : 2052 - 2054
[37] HETEROCHROMATIC REGIONS ON CHROMOSOME-1, CHROMOSOME-9, CHROMOSOME-16, AND CHROMOSOME-Y IN CHILDREN WITH SOME DISTURBANCES OCCURRING DURING EMBRYO DEVELOPMENT
PODUGOLNIKOVA, OA
BLUMINA, MG
HUMAN GENETICS, 1983, 63 (02) : 183 - 188
[38] CENTROMERIC HETEROCHROMATIN INSTABILITY OF CHROMOSOME-1, CHROMOSOME-9, AND CHROMOSOME-16 IN VARIABLE IMMUNODEFICIENCY SYNDROME - A VIRUS-INDUCED PHENOMENON
HAAS, OA
HUMAN GENETICS, 1990, 85 (02) : 244 - 246
[39] INVESTIGATION OF THE CHROMOSOME-9 AND CHROMOSOME-16 TUBEROUS SCLEROSIS LOCI BY HAPLOTYPE ANALYSIS
BROOKCARTER, PB
DANIELS, I
NELLIST, M
KWIATKOWSKI, D
JANSSEN, LAJ
JANSSEN, ALWH
VERHOEF, S
LINDHOUT, D
HALLEY, DJJ
SAMPSON, JR
CYTOGENETICS AND CELL GENETICS, 1993, 64 (02): : 109 - 109
[40] C-BAND POLYMORPHISMS OF CHROMOSOME-1, CHROMOSOME-9, AND CHROMOSOME-16 IN 4 SUBGROUPS OF MENTALLY-RETARDED PATIENTS AND A NORMAL CONTROL POPULATION
WANG, HS
HAMERTON, JL
HUMAN GENETICS, 1979, 51 (03) : 269 - 275

← 1 2 3 4 5 →