(Q68293112)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

title

A molecular genetic approach to the identification of isochromosomes of chromosome 21 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

main subject

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1671850

25 October 2022

1 reference

25 October 2022

author name string

L. G. Shaffer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1671850

25 October 2022

C. K. Jackson-Cook

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1671850

25 October 2022

J. M. Meyer

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1671850

25 October 2022

J. A. Brown

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1671850

25 October 2022

J. E. Spence

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1671850

25 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1671850

25 October 2022

publication date

1 February 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

23 September 2019

http://link.springer.com/content/pdf/10.1007/BF00201838.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00201838/fulltext.html

25 October 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF00201838

25 October 2022

1 reference

25 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

volume

86

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

page(s)

375-382

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysis

23 September 2019

cites work

1 reference

12 December 2020

De novo 21/21 translocation Down syndrome. Studies of parental origin of the translocation and acrocentric associations in parents

1 reference

12 December 2020

Origin of human trisomics and polyploids

1 reference

12 December 2020

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

1 reference

12 December 2020

On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms

1 reference

12 December 2020

The probability of detecting the origin of nondisjunction of autosomal trisomies

1 reference

12 December 2020

Origin of the extra chromosome in trisomy 21

1 reference

12 December 2020

Isochromosome not translocation in trisomy 21q21q

1 reference

12 December 2020

Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism

1 reference

12 December 2020

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

1 reference

12 December 2020

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

12 December 2020

The use of DNA probes to establish parental origin in Down syndrome

1 reference

12 December 2020

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

12 December 2020

The parental origin and mechanism of formation of three dicentric X chromosomes

1 reference

12 December 2020

Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome

1 reference

12 December 2020

Parental origin of de novo chromosome rearrangements

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

The origin of isochromosomes.

1 reference

12 December 2020

Molecular evidence for true isochromosome 21q

1 reference

12 December 2020

Genetic linkage map of human chromosome 21

1 reference

12 December 2020

Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis

1 reference

12 December 2020

Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of origin

1 reference

12 December 2020

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

1 reference

12 December 2020

Structural chromosome abnormalities in Down syndrome: a study of two families

1 reference

12 December 2020

How do human isochromosomes arise?

1 reference

12 December 2020

Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping

1 reference

12 December 2020

Two cases of Down syndrome with unusual de novo translocation*

1 reference

12 December 2020

A genetic linkage map of 17 markers on human chromosome 21

1 reference

12 December 2020

High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms

1 reference

12 December 2020

Parental origin of the extra chromosome in Down's syndrome

1 reference

12 December 2020

The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations

1 reference

12 December 2020

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

12 December 2020

Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction

1 reference

12 December 2020

Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

1 reference

12 December 2020

Nucleolar organizer region variants as a risk factor for Down syndrome

1 reference

12 December 2020

Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome

1 reference

12 December 2020

Morphology alone does not make an isochromosome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00201838

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1671850%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

1 reference