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PMID: 14207553 Published · ppublish English Journal Article

TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

American journal of human genetics ·Vol. 16 ·1964-09-00 ·Pages 380-92

NANCE WE, UCHIDA I

Abstract

暂无摘要

Keywords
BLOOD GROUPS ELECTROPHORESIS GENETICS HUMAN GLUCOSEPHOSPHATE DEHYDROGENASE MONGOLISM STATISTICS TURNER'S SYNDROME TWINS
MeSH Terms
Blood Group Antigens Down Syndrome Electrophoresis Genetics, Medical Glucosephosphate Dehydrogenase Humans Statistics as Topic Turner Syndrome Twins
Chemicals
Blood Group Antigens Glucosephosphate Dehydrogenase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
NANCE W E
UCHIDA I
References (17)
17 references, click to expand
  1. A genetic study of a defect in glutathione metabolism of the erythrocyte.
    Bull Johns Hopkins Hosp. 1958 Jan;102(1):21-37 PMID: 13500095
  2. Twins: an introduction to gemellology.
    Medicine (Baltimore). 1959 Dec;38:403-14 PMID: 14425951
  3. [Chromosomal detection of a human artificial mosaic].
    C R Hebd Seances Acad Sci. 1961 May 15;252:3148-50 PMID: 13760632
  4. THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS.
    J Pediatr. 1963 Oct;63:577-88 PMID: 14074416
  5. Glucose-6-phosphate dehydrogenase deficiency in an XO individual.
    Cytogenetics. 1962;1:1-4 PMID: 13897100
  6. Sex-linked electrophoretic difference in glucose-6-phosphate dehydrogenase.
    Am J Hum Genet. 1963 Sep;15:241-58 PMID: 14033020
  7. Autosomal cytogenetics.
    Helv Paediatr Acta. 1961 Dec;16:670-90 PMID: 14010092
  8. CHROMOSOME STUDIES IN ABORTUSES AND STILLBORN INFANTS.
    Lancet. 1963 Sep 21;2(7308):603-6 PMID: 14050879
  9. The D triisomy syndrome and XO gonadal dysgenesis in two sisters.
    Am J Hum Genet. 1961 Jun;13:193-204 PMID: 13776246
  10. Electrophoretic heterogeneity of glucose-6-phosphate dehydrogenase and its relationship to enzyme deficiency in man.
    Proc Natl Acad Sci U S A. 1962 Oct 15;48:1868-76 PMID: 14014720
  11. LACTIC DEHYDROGENASE: GENETIC CONTROL IN MAN.
    Science. 1963 Nov 22;142(3595):1075-7 PMID: 14068226
  12. Secular changes in rates of multiple births in the United States.
    Am J Hum Genet. 1962 Dec;14:410-25 PMID: 14028923
  13. Validity of electrophoretic determination of lactic dehydrogenase isozymes.
    Nature. 1963 Jun 1;198:888-9 PMID: 13981748
  14. The causes of mongolism.
    Dan Med Bull. 1956 Aug;3(5):158-64 PMID: 13356619
  15. FACTORS INFLUENCING THE ELECTROPHORETIC MIGRATION OF LACTIC DEHYDROGENASE ISOZYMES.
    J Lab Clin Med. 1963 Oct;62:571-8 PMID: 14080856
  16. Ovarian dysgenesis in identical twins: discrepancy between nuclear chromatin pattern in somatic cells and in blood cells.
    J Clin Endocrinol Metab. 1962 Jun;22:660-5 PMID: 13923207
  17. Source of the X in XO females: the evidence of Xg.
    Lancet. 1963 Mar 9;1(7280):558-9 PMID: 13930841
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1964-09-00
Pages
380-92
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1932469
Subset
OM
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