(Q35441030)

8 August 2017

1 reference

title

Small supernumerary marker chromosomes and uniparental disomy have a story to tell (English)

1 reference

8 August 2017

Thomas Liehr

1

1 reference

8 August 2017

Elisabeth Ewers

2

1 reference

8 August 2017

Ahmed B Hamid

3

1 reference

8 August 2017

Nadezda Kosyakova

4

1 reference

8 August 2017

Martin Voigt

5

1 reference

8 August 2017

Anja Weise

6

1 reference

8 August 2017

Marina Manvelyan

7

1 reference

8 August 2017

publication date

14 June 2011

1 reference

Journal of Histochemistry and Cytochemistry

8 August 2017

published in

1 reference

8 August 2017

volume

59

1 reference

8 August 2017

issue

9

1 reference

8 August 2017

page(s)

842-848

1 reference

Somatic mosaicism in cases with small supernumerary marker chromosomes

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Cytogenetic contribution to uniparental disomy (UPD).

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Small supernumerary marker chromosomes (sSMCs): a spotlight on some nomenclature problems

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Uniparental disomy in cancer

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Small supernumerary marker chromosomes (sSMC) in humans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Molecular biology of Beckwith-Wiedemann syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Face and gaze processing in Prader-Willi syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Diagnostic proceeding in Silver-Russell syndrome.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

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

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1369%2F0022155411412780

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3201165

Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21673185

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A new genetic concept: uniparental disomy and its potential effect, isodisomy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21673185

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1369/0022155411412780

1 reference

8 August 2017

1 reference

8 August 2017

1 reference