(Q47654481)

English

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

scientific article published in January 2004

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scholarly article

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

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

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

0 references

author name string

T Liehr

1

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

G Hickmann

2

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

P Kozlowski

3

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

U Claussen

4

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

H Starke

5

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

publication date

1 January 2004

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

Chromosome Research

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

12

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

3

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

239-244

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

https://scigraph.springernature.com/pub.10.1023/b:chro.0000021916.18019.1c

0 references

Analphoid 3qter markers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotyping of human synaptonemal complexes by cenM-FISH

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic supernumerary marker chromosome identified as a der(3) by FISH

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

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/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pericentromeric euchromatin is conserved in minute human supernumerary chromosomes: a study using cross-species colour segmenting (RxFISH).

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A neocentromere on human chromosome 3 without detectable alpha-satellite DNA forms morphologically normal kinetochores

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An analphoid supernumerary marker chromosome derived from chromosome 3 ascertained in a fetus with multiple malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic Approaches

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal supernumerary r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A search for uniparental disomy in carriers of supernumerary marker chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

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/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incomplete trisomy in a mongoloid child exhibiting minimal stigmata

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First patient with trisomy 21 accompanied by an additional der(4)(:p11 ? q11:) plus partial uniparental disomy 4p15-16

1 reference

https://pubmed.ncbi.nlm.nih.gov/15125637

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/15125637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/B:CHRO.0000021916.18019.1C

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/15125637

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