(Q36882049)

English

Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report

scientific article published on 14 August 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Lihadh Al-Gazali

11

object named as

Lihadh Al-Gazali

1 reference

Europe PubMed Central

16 August 2017

PMC publication ID

author name string

Sabita K Murthy

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Ashok K Malhotra

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Preenu S Jacob

3

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Sehba Naveed

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Eman Em Al-Rowaished

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Sara Mani

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Shabeer Padariyakam

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

R Pramathan

8

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Ravi Nath

9

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Mahmoud Taleb Al-Ali

10

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

publication date

14 August 2008

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Molecular Cytogenetics

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

19

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

https://scigraph.springernature.com/pub.10.1186/1755-8166-1-19

0 references

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

29 September 2017

Centromere DNA dynamics: latent centromeres and neocentromere formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

27 June 2018

Forty four probands with an additional "marker" chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

27 June 2018

A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

4 September 2018

Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

4 September 2018

Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

4 September 2018

Analphoid 3qter markers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2538529

4 December 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18700989

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/18700989

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/18700989

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1755-8166-1-19

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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