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1
Genetic characteristics of families of XO and XXY patients, including evidence of source of X chromosomes in 7 aneuploid patients.XO和XXY患者家系的遗传特征，包括7例非整倍体患者X染色体来源的证据。
J Med Genet. 1968 Sep;5(3):173-80. doi: 10.1136/jmg.5.3.173.
2
Behavior genetics: principles, methods and examples from XO, XXY and XYY syndromes.
Semin Psychiatry. 1970 Feb;2(1):11-29.
3
Gonosomal aberrations and congenital dyschromatopsias.
Mod Probl Ophthalmol. 1974;13(0):231-47.
4
[Discussion of the paternal origin of the X of a protanopic and Xg(a--) XO Turner syndrome. New numerical estimation].[关于一名红色盲和Xg(a--)XO特纳综合征患者X染色体父源起源的讨论。新的数值估计]
C R Acad Hebd Seances Acad Sci D. 1965 Aug 2;261(5):1381-3.
5
[Color blindness (daltonism) in the light of genetic studies].
Wiad Lek. 1971 Feb 15;24(4):337-42.
6
[Xg-blood group system. A review].
Ugeskr Laeger. 1967 May 18;129(20):651-4.
7
Some contributions of blood groups to human genetics.
Am J Clin Pathol. 1971 Jun;55(6):635-45.
8
Infertility and chromosome abnormality.不孕与染色体异常。
Oxf Rev Reprod Biol. 1984;6:1-46.
9
Some contributions of blood groups to human genetics.
Am J Clin Pathol. 1971 Jun;55(6):635-45.
10
[Cytogenetic investigations in cases of abnormal sex differentiation and determination].
Ginekol Pol. 1970 Jan;41(1):87-100.

引用本文的文献

1
An aetiological study of 290 XXY males, with special reference to the role of paternal age.
Hum Genet. 1984;68(3):248-53. doi: 10.1007/BF00418395.
2
Comments on patients with sex chromosome aneuploidy: dermatoglyphs, parental ages, Xg a blood group.性染色体非整倍体患者的相关评论：皮纹、父母年龄、Xg血型
J Med Genet. 1970 Dec;7(4):345-50. doi: 10.1136/jmg.7.4.345.
3
Cytogenetic, clinical and genealogical analyses in a series of gonadal dysgenesis patients and their families.对一系列性腺发育不全患者及其家族进行的细胞遗传学、临床和系谱分析。
Humangenetik. 1971;13(2):126-43. doi: 10.1007/BF00295794.
4
Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY.
Humangenetik. 1974 Mar 28;21(4):301-8.
5
Analytic review: nature and origin of males with XX sex chromosomes.分析性综述：具有XX性染色体男性的本质与起源
Am J Hum Genet. 1972 Jan;24(1):71-105.
6
Twins with nonconcordant sexual aneuploidy.具有不一致性性染色体非整倍体的双胞胎。
J Med Genet. 1977 Jun;14(3):226-8. doi: 10.1136/jmg.14.3.226.

本文引用的文献

1
[FAMILIAL OCCURRENCE OF CHROMOSOMAL ABERRATIONS].[染色体畸变的家族性发生]
Helv Paediatr Acta. 1964 Nov;19:444-57.
2
IDENTIFICATION OF THE ORIGIN OF THE X CHROMOSOME(S) IN SEX CHROMOSOME ANEUPLOIDY.
Can J Genet Cytol. 1965 Jun;7:214-22. doi: 10.1139/g65-030.
3
THE XG BLOOD GROUP SYSTEM: DATA ON 294 WHITE FAMILIES, MAINLY CANADIAN.
Can J Genet Cytol. 1964 Dec;6:431-4. doi: 10.1139/g64-056.
4
TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.特纳综合征、双胎妊娠与葡萄糖-6-磷酸脱氢酶的一种罕见变异型
Am J Hum Genet. 1964 Sep;16(3):380-92.
5
[FAMILIAL TURNER'S SYNDROME. STUDY OF 2 FAMILIES WITH XO AND XX KARYOTYPES].
Ann Pediatr (Paris). 1963 Apr 2;10:163-7.
6
PARENTAL AGE AND THE SOURCE OF THE X CHROMOSOMES IN XXY KLINEFELTER'S SYNDROME.
Lancet. 1964 Jan 4;1(7323):46. doi: 10.1016/s0140-6736(64)92198-1.
7
NON-DISJUNCTION AND XXY MEN.不分离与XXY男性。
Lancet. 1963 Nov 23;2(7317):1121-2. doi: 10.1016/s0140-6736(63)92897-6.
8
Parental origin of the sex chromosomes in the XO and XXY karyotypes in man.人类XO和XXY核型中性染色体的亲本来源。
Ann Hum Genet. 1963 Jun;26:297-304. doi: 10.1111/j.1469-1809.1963.tb01325.x.
9
Chromosome preparations of leukocytes cultured from human peripheral blood.从人外周血培养的白细胞的染色体标本制备。
Exp Cell Res. 1960 Sep;20:613-6. doi: 10.1016/0014-4827(60)90138-5.
10
Carbol fuchsin as a stain for human chromosomes.石炭酸复红作为人类染色体的染色剂。
Stain Technol. 1961 Jul;36:233-6. doi: 10.3109/10520296109113278.

Genetic characteristics of families of XO and XXY patients, including evidence of source of X chromosomes in 7 aneuploid patients.

作者信息

Soltan H C

出版信息

J Med Genet. 1968 Sep;5(3):173-80. doi: 10.1136/jmg.5.3.173.

DOI:10.1136/jmg.5.3.173
PMID:5304308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468637/
Abstract
摘要