Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients (Q38462574)

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scientific article published on January 2007

Language	Label	Description	Also known as
English	Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients	scientific article published on January 2007

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Ferdinand von Eggeling

9

object named as

Ferdinand von Eggeling

0 references

Pawel Stankiewicz

4

object named as

Pawel Stankiewicz

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Tadeusz Mazurczak

10

object named as

Tadeusz Mazurczak

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

11

object named as

Ewa Bocian

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

3

object named as

Ewa Obersztyn

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

author name string

Joanna Pietrzak

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Kristin Mrasek

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Nadezda Kosyakova

5

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Anja Weise

6

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Sau Wai Cheung

7

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Wei Wen Cai

8

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Thomas Liehr

12

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

1 January 2007

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Europe PubMed Central

PubMed publication ID

3 September 2017

Journal of Applied Genetics

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Europe PubMed Central

PubMed publication ID

3 September 2017

48

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Europe PubMed Central

PubMed publication ID

3 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

167-175

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Preferential involvement of the short arm in chromosome 8-derived supernumerary markers and ring as identified by chromosome arm painting

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Characterization of mosaic supernumerary ring chromosomes by array-CGH: segmental aneusomy for proximal 4q in a child with tall stature and obesity.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Forty four probands with an additional "marker" chromosome.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Familial partial trisomy 8p without dysmorphic features and only mild mental retardation

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Supernumerary marker chromosomes (SMC) and uniparental disomy (UPD): coincidence or consequence?

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

AcroM fluorescent in situ hybridization analyses of marker chromosomes

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Small supernumerary marker chromosomes (sSMC) in humans

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Two new cases of analphoid marker chromosomes.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Marker chromosome 21 identified by microdissection and FISH.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Identification and molecular characterization of a de novo supernumerary ring chromosome 18 in a patient with Klippel-Trenaunay syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Inv dup(15) supernumerary marker chromosomes

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

High-resolution Human Genome Scanning Using Whole-genome BAC Arrays

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism

1 reference

https://api.crossref.org/works/10.1007%2FBF03194675

21 January 2018

[Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations]

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Forty-two supernumerary marker chromosomes (SMCs) in 43,273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delineation of supernumerary marker chromosomes in 38 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal phenotype and partial trisomy for the G positive region of chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microdissection based high resolution multicolor banding for all 24 human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multicolor FISH probe sets and their applications

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a ring chromosome as a ring 8 using fluorescent in situ hybridization (FISH) in a child with multiple congenital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a small supernumerary ring marker derived from chromosome 2 by forward and reverse chromosome painting

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Free proximal trisomy 21 without the Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/17495351

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03194675

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

ResearchGate publication ID

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