(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

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Europe PubMed Central

PubMed publication ID

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

PubMed publication ID

14 September 2017

1 reference

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author name string

U Langenbeck

1

1 reference

Europe PubMed Central

PubMed publication ID

14 September 2017

I Hansmann

2

1 reference

Europe PubMed Central

PubMed publication ID

14 September 2017

B Hinney

3

1 reference

Europe PubMed Central

PubMed publication ID

14 September 2017

V Hönig

4

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Europe PubMed Central

PubMed publication ID

14 September 2017

publication date

1 July 1976

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Europe PubMed Central

PubMed publication ID

14 September 2017

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Europe PubMed Central

PubMed publication ID

14 September 2017

33

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Europe PubMed Central

PubMed publication ID

14 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

14 September 2017

89-102

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Europe PubMed Central

PubMed publication ID

14 September 2017

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

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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

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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

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A sex-linked blood group

1 reference

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

12 December 2020

based on heuristic

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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

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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

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Xg and sex-chromosome abnormalities

1 reference

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

12 December 2020

based on heuristic

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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

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Induced chromosome aberrations in unfertilized oocytes of mice

1 reference

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

12 December 2020

based on heuristic

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Centrometric linkage in autosomal trisomies

1 reference

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

12 December 2020

based on heuristic

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Human Q and C chromosomal variations: distribution and incidence

1 reference

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

12 December 2020

based on heuristic

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Origin of extra chromosome in trisomy 21

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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Esterase D: a new human polymorphism

1 reference

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

12 December 2020

based on heuristic

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Centromeric linkage in trisomy 21

1 reference

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

12 December 2020

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Chiasma and univalent frequencies in aging female mice

1 reference

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

12 December 2020

based on heuristic

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Origin of the trisomic 21 chromosome

1 reference

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

12 December 2020

based on heuristic

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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

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Chiasma frequency and maternal age in mammals.

1 reference

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

12 December 2020

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[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

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Origin of extra chromosome in trisomy 21

1 reference

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

12 December 2020

based on heuristic

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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

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The nucleolus, virus infection, and trisomy in man.

1 reference

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

12 December 2020

based on heuristic

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Chromosome abnormalities in rabbit blastocysts following delayed fertilization

1 reference

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

12 December 2020

based on heuristic

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Chromatid disjunction in unfertilized ageing oocytes.

1 reference

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

12 December 2020

based on heuristic

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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

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[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

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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

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A Mongol girl with 46 chromosomes

1 reference

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

12 December 2020

based on heuristic

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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

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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

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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

PubMed publication ID

14 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 September 2017

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