A familial variant of chromosome 9.
作者信息
Palmer C G, Schroder J
出版信息
J Med Genet. 1971 Jun;8(2):202-8. doi: 10.1136/jmg.8.2.202.
Abstract
摘要
相似文献
1
A familial variant of chromosome 9.
J Med Genet. 1971 Jun;8(2):202-8. doi: 10.1136/jmg.8.2.202.
2
The distribution and localization of drug-induced secondary constrictions in human chromosomes.
Can J Genet Cytol. 1972 Mar;14(1):81-93. doi: 10.1139/g72-011.
3
An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
Hum Hered. 1973;23(6):568-85. doi: 10.1159/000152624.
4
Presumptive C-15 translocation and familial large Y identified by autoradiography.
J Med Genet. 1969 Mar;6(1):89-94. doi: 10.1136/jmg.6.1.89.
5
6
[Abnormal C group chromosome in several members of the same family].
Humangenetik. 1968;6(4):326-34.
7
Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
Sov Genet. 1974 Jun 1;8(5):651-7.
8
Distribution of mitomycin C-induced damage in human chromosomes with special reference to regions of repetitive DNA.
Chromosoma. 1974;48(2):203-11. doi: 10.1007/BF00283964.
9
Structural variation in human nitotic chromosomes.
Ann Acad Sci Fenn Biol. 1971;179:1-69.
10
[Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation].
Ann Genet. 1969 Jun;12(2):133-7.
引用本文的文献
1
Partial inversion of the secondary constriction of chromosome 9. Does it exist?
Hum Genet. 1981;59(4):310-6. doi: 10.1007/BF00295463.
2
The quantitative analysis of constitutive heterochromatic regions of human chromosomes 1, 9, and 16 in relation to size and inversion heteromorphisms in East Indians.
Experientia. 1982 Mar 15;38(3):324-6. doi: 10.1007/BF01949370.
3
Aspects of evaluation, significance, and evolution of human C-band heteromorphism.
Hum Genet. 1982;61(4):281-94. doi: 10.1007/BF00276592.
4
[Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations (author's transl)].
Humangenetik. 1973 Dec 10;20(3):273-82. doi: 10.1007/BF00385740.
5
Utilization of somatic cell hybrids for genetic studies in man.
Humangenetik. 1973;19(1):1-40. doi: 10.1007/BF00295233.
6
Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.
Humangenetik. 1974;21(3):211-6. doi: 10.1007/BF00279014.
7
The segregation of C-band polymorphisms on chromosomes 1, 9, and 16.
Am J Hum Genet. 1976 Jul;28(4):412-6.
本文引用的文献
1
The Effect of Abnormal Chromosome 10 on Preferential Segregation and Crossing over in Maize.
Genetics. 1966 May;53(5):989-1020. doi: 10.1093/genetics/53.5.989.
2
A Genetic Study of Segregation in a Translocation Heterozygote in Drosophila.
Genetics. 1955 Nov;40(6):809-25. doi: 10.1093/genetics/40.6.809.
3
EFFECTS OF MITOMYCIN C ON HUMAN CHROMOSOMES.
J Cell Biol. 1964 Nov;23(2):386-95. doi: 10.1083/jcb.23.2.386.
4
PREFERENTIAL SEGREGATION OF CHROMOSOMES FROM A TRIVALENT IN HAPLOPAPPUS GRACILIS.
Science. 1964 Jul 31;145(3631):511-3. doi: 10.1126/science.145.3631.511.
5
THE EFFECT OF 5-BROMODEOXYURIDINE ON HUMAN CHROMOSOMES.
Exp Cell Res. 1964 Mar;34:182-6. doi: 10.1016/0014-4827(64)90193-4.
6
A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION.
Am J Hum Genet. 1963 Dec;15(4):465-75.
7
Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.
Chromosoma. 1963;14:146-53. doi: 10.1007/BF00336756.
8
Enhancement of secondary constrictions and the heterochromatic X in human cells.
Cytogenetics. 1962;1:225-44. doi: 10.1159/000129733.
9
Sequential tests for the detection of linkage.
Am J Hum Genet. 1955 Sep;7(3):277-318.
10
The idiogram of the sheep with particular reference to secondary constrictions.
Can J Genet Cytol. 1967 Sep;9(3):543-53. doi: 10.1139/g67-058.
Zotero 插件