Nucleolar organizer region variants as a risk factor for Down syndrome (Q35200688)

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7 October 2019

title

Nucleolar organizer region variants as a risk factor for Down syndrome (English)

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7 October 2019

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C K Jackson-Cook

1

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7 October 2019

D B Flannery

2

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7 October 2019

L A Corey

3

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7 October 2019

W E Nance

4

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7 October 2019

J A Brown

5

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7 October 2019

language of work or name

English

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publication date

1 November 1985

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7 October 2019

number of pages

13

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American Journal of Human Genetics

inferred from page(s)

published in

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7 October 2019

volume

37

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7 October 2019

issue

6

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7 October 2019

page(s)

1049-1061

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Chromosome preparations of leukocytes cultured from human peripheral blood

7 October 2019

cites work

1 reference

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Human inherited marker chromosome 22 short-arm enlargement: investigation of rDNA gene multiplicity, Ag-band size, and acrocentric association

13 July 2018

1 reference

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Association of ribosomal genes in the fibrillar center of the nucleolus: a factor influencing translocation and nondisjunction in the human meiotic oocyte

13 July 2018

1 reference

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Temporal increase in the rate of Down syndrome livebirths to older mothers in New York State.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

13 July 2018

1 reference

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Intercalar satellites of human acrocentric chromosomes as a cytological manifestation of polymorphism in GC-rich material?

13 July 2018

1 reference

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Short arm enlargement in acrocentric chromosomes.

13 July 2018

1 reference

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Origin of human trisomics and polyploids

13 July 2018

1 reference

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The origin of the extra chromosome 21 in Down syndrome. Studies of fluorescent variants and satelite association in 26 informative families

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

Evidence for the inheritance of silver-stained nucleolus organizer regions

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

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

13 July 2018

1 reference

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Localization of the nucleolar organizer by computer-aided analysis of a variant no. 21 in a human isolate

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

Cytological analyses of a 14p+variant by means of N-banding and combinations of silver staining and chromosome bandings

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

Frequency of satellite association of human chromosomes is correlated with amount of Ag-staining of the nucleolus organizer region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

N-Band polymorphism of human acrocentric chromosomes and its relevance to satellite association

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684740

Nucleolus organizer and N-band distribution in morphologic and fluorescence variants of human chromosomes

13 July 2018

1 reference

12 December 2020

Regulation of rRNA gene expression in a human familial 14p+ marker chromosome

1 reference

12 December 2020

Chromosome heteromorphisms in the Japanese. II. Nucleolus organizer regions of variant chromosomes in D and G groups

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12 December 2020

Non-disjunction in trisomy 21: study of chromosomal heteromorphisms in 110 families

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12 December 2020

Is it always the same NOR that is more active in a pair of acrocentrics with distinct AG-stainings?

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12 December 2020

Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome

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12 December 2020

The origin of human trisomy: a study of heteromorphisms and satellite associations

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12 December 2020

Polymorphisms of Ag-stained nucleolar organizer regions in man

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12 December 2020

Parental origin of the extra chromosome in Down's Syndrome

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12 December 2020

Stain intensity of human nucleolus organizer region reflects incorporation of uridine into mature ribosomal RNA

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12 December 2020

Silver staining of nucleolus organizer regions during human spermatogenesis

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12 December 2020

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12 December 2020

CHROMOSOME STUDIES IN MONGOLOIDS AND THEIR FAMILIES

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12 December 2020

THE SITES OF NUCLEOLUS FORMATION IN HUMAN PACHYTENE CHROMOSOMES

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12 December 2020

ENLARGED SHORT ARM OF A SMALL ACROCENTRIC CHROMOSOME IN GRANDFATHER, MOTHER AND CHILD, THE LATTER WITH DOWN'S SYNDROME

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12 December 2020

A marker chromosome number 14 with double satellite obseved in two generations: an unbalanced chromosome constitution associated with normal phenotype

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12 December 2020

Antenatal genetic diagnosis in a kindred with a 15p plus chromosome

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12 December 2020

Trisomy 18 and 21 in two siblings

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12 December 2020

On the relationship between the frequency of association and the nucleolar constriction of individual acrocentric chromosomes

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12 December 2020

Quantitative studies on the arrangement of human metaphase chromosomes. IV. The association frequency of human acrocentric marker chromosomes

1 reference

12 December 2020

Cytogenetic studies in families with two 47, +21-siblings

1 reference

12 December 2020

Satellite-association frequency and rDNA content of a double-satellited chromosome

1 reference

12 December 2020

Variation in the number of genes for rRNA among human acrocentric chromosomes: correlation with frequency of satellite association

1 reference

12 December 2020

Identifiers

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2934977%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

PubMed publication ID

2934977

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