(Q36645370)

15 August 2017

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

1 reference

15 August 2017

Vladimir Trifonov

1

1 reference

15 August 2017

Simon Fluri

2

1 reference

15 August 2017

Franz Binkert

3

1 reference

15 August 2017

Adayapalam Nandini

4

1 reference

15 August 2017

Jasen Anderson

5

1 reference

15 August 2017

Laura Rodriguez

6

1 reference

15 August 2017

Madeleine Gross

7

1 reference

15 August 2017

Nadezda Kosyakova

8

1 reference

15 August 2017

Hasmik Mkrtchyan

9

1 reference

15 August 2017

Elisabeth Ewers

10

1 reference

15 August 2017

Daniela Reich

11

1 reference

15 August 2017

Anja Weise

12

1 reference

15 August 2017

Thomas Liehr

13

1 reference

15 August 2017

15 April 2008

1 reference

15 August 2017

Molecular Cytogenetics

1 reference

15 August 2017

1

1 reference

15 August 2017

6

1 reference

Array painting using microdissected chromosomes to map chromosomal breakpoints

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

Small supernumerary marker chromosomes (sSMC) in humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

Microdissection based high resolution multicolor banding for all 24 human chromosomes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardation.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

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

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375881

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

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18471318

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18471318

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Distribution of the D15Z1 copy number polymorphism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18471318

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1755-8166-1-6

1 reference

Dimensions Publication ID

15 August 2017

0 references

1 reference

15 August 2017

PubMed publication ID

18471318

1 reference