(Q74243433)

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

scientific article published on 01 February 1998

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9 November 2019

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

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Europe PubMed Central

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9 November 2019

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fluorescence in situ hybridization

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10 December 2024

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J. A. Crolla

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10 December 2024

F. Long

2

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10 December 2024

H. Rivera

3

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10 December 2024

N. R. Dennis

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10 December 2024

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10 December 2024

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1 February 1998

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9 November 2019

3 February 1998

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National Center for Biotechnology Information

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10 December 2024

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10.1002/(SICI)1096-8628(19980203)75:4<355::AID-AJMG4>3.0.CO;2-P

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10 December 2024

https://onlinelibrary.wiley.com/doi/full/10.1002/(SICI)1096-8628(19980203)75:4%3C355::AID-AJMG4%3E3.0.CO;2-P

1 reference

10.1002/(SICI)1096-8628(19980203)75:4<355::AID-AJMG4>3.0.CO;2-P

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10 December 2024

American Journal of Medical Genetics Part A

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9 November 2019

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9 November 2019

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9 November 2019

355-366

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9 November 2019

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

1 reference

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21 January 2018

Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization

1 reference

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21 January 2018

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

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21 January 2018

Forty four probands with an additional "marker" chromosome

1 reference

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21 January 2018

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

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21 January 2018

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

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21 January 2018

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics

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21 January 2018

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

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Identification of marker chromosomes in thirteen patients using FISH probing

1 reference

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21 January 2018

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation

1 reference

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21 January 2018

Bisatellited extra small metacentric chromosome in newborns

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21 January 2018

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

1 reference

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21 January 2018

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

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Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

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Characterization of the supernumerary chromosome in cat eye syndrome

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A simple salting out procedure for extracting DNA from human nucleated cells

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

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21 January 2018

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)

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Chromosome studies. I. Taxonomic relationships shown in the chromosomes of tettigidae and acrididae: V-shaped chromosomes and their significance in acrididae, locustidae, and gryllidae: Chromosomes and variation

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21 January 2018

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome

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

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Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

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An imprinted gene(s) for diabetes?

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A search for uniparental disomy in carriers of supernumerary marker chromosomes

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

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

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10 December 2024

Identifiers

10.1002/(SICI)1096-8628(19980203)75:4<355::AID-AJMG4>3.0.CO;2-P

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482641%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482641%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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