Home LiteratureArticle Details
PMID: 5304308 Published · ppublish English Journal Article

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

Journal of medical genetics ·Vol. 5 ·No. 3 ·1968-09-00 ·Pages 173-80

Soltan HC

Abstract

暂无摘要

MeSH Terms
Abortion, Spontaneous Adolescent Adult Blood Group Antigens Color Vision Defects/genetics Female Fetal Death Humans Klinefelter Syndrome/genetics Male Maternal Age Pedigree Pregnancy Sex Chromatin Sex Ratio Turner Syndrome/genetics Twins
Chemicals
Blood Group Antigens
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Soltan H C
References (14)
14 references, click to expand
  1. [Klinefelter's syndrome in children of mothers with sex chromosome anomalies].
    Helv Paediatr Acta. 1965 Sep;20(4):359-68 PMID: 5862851
  2. Twins in sibships with Klinefelter's syndrome.
    J Med Genet. 1966 Jun;3(2):114-6 PMID: 6007032
  3. [Discrepancy between findings on chromatin & genetic sex in the Klinefelter syndrome].
    Acta Endocrinol (Copenh). 1959 Feb;30(2):296-320 PMID: 13616929
  4. Colour-blindness in Klinefelter's syndrome.
    Nature. 1959 May 23;183(4673):1452-3 PMID: 13657163
  5. Carbol fuchsin as a stain for human chromosomes.
    Stain Technol. 1961 Jul;36:233-6 PMID: 13690989
  6. Chromosome preparations of leukocytes cultured from human peripheral blood.
    Exp Cell Res. 1960 Sep;20:613-6 PMID: 13772379
  7. Parental origin of the sex chromosomes in the XO and XXY karyotypes in man.
    Ann Hum Genet. 1963 Jun;26:297-304 PMID: 13959333
  8. NON-DISJUNCTION AND XXY MEN.
    Lancet. 1963 Nov 23;2(7317):1121-2 PMID: 14063437
  9. PARENTAL AGE AND THE SOURCE OF THE X CHROMOSOMES IN XXY KLINEFELTER'S SYNDROME.
    Lancet. 1964 Jan 4;1(7323):46 PMID: 14072905
  10. TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.
    Am J Hum Genet. 1964 Sep;16:380-92 PMID: 14207553
  11. THE XG BLOOD GROUP SYSTEM: DATA ON 294 WHITE FAMILIES, MAINLY CANADIAN.
    Can J Genet Cytol. 1964 Dec;6:431-4 PMID: 14244732
  12. IDENTIFICATION OF THE ORIGIN OF THE X CHROMOSOME(S) IN SEX CHROMOSOME ANEUPLOIDY.
    Can J Genet Cytol. 1965 Jun;7:214-22 PMID: 14324865
  13. [FAMILIAL TURNER'S SYNDROME. STUDY OF 2 FAMILIES WITH XO AND XX KARYOTYPES].
    Ann Pediatr (Paris). 1963 Apr 2;10:163-7 PMID: 14122073
  14. [FAMILIAL OCCURRENCE OF CHROMOSOMAL ABERRATIONS].
    Helv Paediatr Acta. 1964 Nov;19:444-57 PMID: 14337174
Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
DOI
10.1136/jmg.5.3.173
Published
1968-09-00
Pages
173-80
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1468637
Subset
IM
External Links
PubMed source DOI: 10.1136/jmg.5.3.173 PMC Full Text View journal details
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com

Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2