(Q80914628)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15508017%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited (English)

1 reference

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4 January 2020

author name string

John A Crolla

1

1 reference

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4 January 2020

Sheila A Youings

2

1 reference

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4 January 2020

Sarah Ennis

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15508017%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Patricia A Jacobs

4

1 reference

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4 January 2020

publication date

1 February 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15508017%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

4 January 2020

published in

1 reference

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4 January 2020

volume

13

1 reference

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4 January 2020

issue

2

1 reference

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4 January 2020

page(s)

154-160

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201311

4 January 2020

exact match

0 references

cites work

Forty four probands with an additional "marker" chromosome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Bisatellited extra small metacentric chromosome in newborns

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Supernumerary marker 15 chromosomes: a clinical, molecular and FISH approach to diagnosis and prognosis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effect

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Characterization of the supernumerary chromosome in cat eye syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Inv dup(15) supernumerary marker chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

A 10-year survey, 1980-1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12,699 prenatal samples

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Clinical and molecular analysis of five inv dup(15) patients.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Molecular and Fluorescence In Situ Hybridization Characterization of the Breakpoints in 46 Large Supernumerary Marker 15 Chromosomes Reveals an Unexpected Level of Complexity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Cytogenetic and age-dependent risk factors associated with uniparental disomy 15

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Maternal origin of inv dup(15) chromosomes in infantile autism.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201311

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201311

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15508017%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference