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PMID: 131104 Published · ppublish English Journal Article

Origin of the extra chromosome no. 21 in Down's syndrome.

Human genetics ·Vol. 32 ·No. 1 ·1976-04-15 ·Pages 13-6

Wagenbichler P, Killian W, Rett A, Schnedl W

Abstract

Eighteen of 38 examined families with children with Down's syndrome showed polymorphisms of chromosome 21 elucidating the origin of the extra chromosome 21. Maternal origin was found in 10 cases and paternal origin in 8 cases. In both sexes errors occurred both in the first and in the second meiotic division.

MeSH Terms
Adult Age Factors Chromosomes, Human, 21-22 and Y Down Syndrome/genetics Female Humans Male Meiosis Middle Aged Parents Pedigree Polymorphism, Genetic Sex Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wagenbichler P
Killian W
Rett A
Schnedl W
References (6)
6 references, click to expand
  1. Analysis of the human karyotype by the recent banding techniques.
    Arch Genet (Zur). 1973;46(2):65-98 PMID: 4131243
  2. Difference in fluorescence of the homologe chromosomes No. 3 in man.
    Humangenetik. 1971;12(1):59-63 PMID: 4104179
  3. Trisomy 21 in man due to maternal non-disjunction during the first meiotic division.
    Hereditas. 1972;70(1):153-4 PMID: 4281765
  4. Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.
    Am J Hum Genet. 1975 Mar;27(2):178-89 PMID: 47710
  5. Origin of the trisomic 21 chromosome.
    Lancet. 1973 Feb 17;1(7799):375 PMID: 4121971
  6. Origin of extra chromosome in trisomy 21.
    Lancet. 1973 Jan 20;1(7795):131-3 PMID: 4118469
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1976-04-15
Pages
13-6
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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