(Q39775569)

English

On the origin of the supernumerary chromosome in autosomal trisomies--with special reference to Down's syndrome. A bias in tracing nondisjunction by chromosomal and biochemical polymorphisms

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

14 September 2017

On the origin of the supernumerary chromosome in autosomal trisomies--with special reference to Down's syndrome. A bias in tracing nondisjunction by chromosomal and biochemical polymorphisms (English)

1 reference

Europe PubMed Central

14 September 2017

1 reference

based on heuristic

inferred from title

author name string

U Langenbeck

1

1 reference

Europe PubMed Central

14 September 2017

I Hansmann

2

1 reference

Europe PubMed Central

14 September 2017

B Hinney

3

1 reference

Europe PubMed Central

14 September 2017

V Hönig

4

1 reference

Europe PubMed Central

14 September 2017

publication date

1 July 1976

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

33

1 reference

Europe PubMed Central

14 September 2017

89-102

1 reference

Europe PubMed Central

14 September 2017

2

1 reference

Europe PubMed Central

14 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00281882

0 references

Analysis of the human karyotype by the recent banding techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A search for linkage between the Ag and (dimeric) superoxide dismutase (SOD-1) loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A sex-linked blood group

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescent chromosome polymorphisms: frequencies and segregations in a Dutch population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xg and sex-chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21 in man due to maternal non-disjunction during the first meiotic division

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Induced chromosome aberrations in unfertilized oocytes of mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centrometric linkage in autosomal trisomies

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Q and C chromosomal variations: distribution and incidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of extra chromosome in trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Discrepancy between chromatin finding and chromosomal sex in Klinefelter's syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Esterase D: a new human polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Centromeric linkage in trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiasma and univalent frequencies in aging female mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of the trisomic 21 chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

21 p-maternal in duplicate in a case of trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiasma frequency and maternal age in mammals.

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Esterase D polymorphism: demonstration by high-voltage, starch-gel electrophoresis and presentation of allele frequencies (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of extra chromosome in trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of non-disjunction of meiotic chromosomes and of degeneration of maturation spindles in eggs affected by intrafollicular overripeness

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The nucleolus, virus infection, and trisomy in man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in rabbit blastocysts following delayed fertilization

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromatid disjunction in unfertilized ageing oocytes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Christchurch chromosome (Gp-). Mongolism, erythroleukemia and an inherited Gp- chromosome (Christchurch)

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Overactivity of the indophenol oxidase (form dimeric) in the trisomy 21, secondary to triplicated gene (author's transl)].

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common polymorphism of Peptidase A. Electrophoretic variants associated with quantitative variation of red cell levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Mongol girl with 46 chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal and paternal origin of extra chromosome in trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relative effects of paternal and maternal age in mongolism. 1933.

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of duplicate 2lp maternal chromosomes in a case of trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delayed fertilization and chromosomal anomalies in mouse embryos

1 reference

https://pubmed.ncbi.nlm.nih.gov/133081

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00281882

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q39775569&oldid=2090212647"