(Q35643076)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

author name string

Robinson WP

1

1 reference

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27 October 2019

Binkert F

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Bernasconi F

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Lorda-Sanchez I

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

Werder EA

5

1 reference

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27 October 2019

Schinzel AA

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

language of work or name

English

0 references

publication date

1 February 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

27 October 2019

published in

1 reference

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27 October 2019

volume

56

1 reference

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27 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

page(s)

444-451

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

Molecular studies of trisomy 18

27 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Uniparental disomy for chromosome 16 in humans.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Exclusively paternal X chromosomes in a girl with short stature

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Nondisjunction of chromosome 15: origin and recombination

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

A somatic origin of homologous Robertsonian translocations and isochromosomes.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Origin of sex chromosome aneuploidy.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Review and hypotheses: somatic mosaicism: observations related to clinical genetics

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Cytogenetic and molecular studies of trisomy 13.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Parental origin of the extra chromosome in trisomy 18.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Molecular studies of non-disjunction in trisomy 16.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Trisomy 21: association between reduced recombination and nondisjunction

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Molecular studies of parental origin and mosaicism in 45,X conceptuses

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

A second-generation linkage map of the human genome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Multiple origins of X chromosome tetrasomy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801123

[Etiology of numerical and structural aberrations of the X chromosome. A study with highly polymorphic DNA markers]

15 November 2018

1 reference

12 December 2020

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)

1 reference

12 December 2020

Paternal nondisjunction in trisomy 21: excess of male patients

1 reference

12 December 2020

Parental origin of the supernumerary chromosome in trisomy 18

1 reference

12 December 2020

Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes

1 reference

12 December 2020

Trisomy 8 mosaicism syndrome

1 reference

12 December 2020

[Mosaicism--Trisomy 8]

1 reference

12 December 2020

Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group

1 reference

12 December 2020

Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism

1 reference

12 December 2020

Reduced recombination and paternal age effect in Klinefelter syndrome

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7847381%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

PubMed publication ID

7847381

1 reference