(Q33678304)

English

Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH.

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH. (English)

1 reference

Europe PubMed Central

28 July 2017

1 reference

based on heuristic

inferred from title

Xavier Estivill i Pallejà

5

1 reference

Europe PubMed Central

28 July 2017

0 references

author name string

Nadal M

1

1 reference

Europe PubMed Central

28 July 2017

Moreno S

2

1 reference

Europe PubMed Central

28 July 2017

Pritchard M

3

1 reference

Europe PubMed Central

28 July 2017

Preciado MA

4

1 reference

Europe PubMed Central

28 July 2017

Ramos-Arroyo MA

6

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

1 January 1997

1 reference

Europe PubMed Central

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

28 July 2017

34

1 reference

Europe PubMed Central

28 July 2017

50-54

1 reference

Europe PubMed Central

28 July 2017

1

1 reference

Europe PubMed Central

28 July 2017

describes a project that uses

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Down syndrome phenotypes: the consequences of chromosomal imbalance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

An integrated YAC-overlap and 'cosmid-pocket' map of the human chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Receptors for human alpha and beta interferon but not for gamma interferon are specified by human chromosome 21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Chromosomal in situ hybridization using yeast artificial chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Continuum of overlapping clones spanning the entire human chromosome 21q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

An optimized Alu-PCR primer pair for human-specific amplification of YACs and somatic cell hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

Ring chromosome 15 syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

21 June 2018

The EUROGEM map of human chromosome 21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050847

30 October 2018

Unbalanced Robertsonian translocations associated with Down's syndrome or Patau's syndrome: chromosome subtype, proportion inherited, mutation rates, and sex ratio

1 reference

https://pubmed.ncbi.nlm.nih.gov/9032650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Linkage Map of Human Chromosome 21: 43 PCR Markers at Average Intervals of 2.5 cM

1 reference

https://pubmed.ncbi.nlm.nih.gov/9032650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A NotI restriction map of the entire long arm of human chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/9032650

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.34.1.50

1 reference

Europe PubMed Central

28 July 2017

release_u5bpxvpomfd7pibnnspbqfwkye

1 reference

https://api.fatcat.wiki/v0/release/u5bpxvpomfd7pibnnspbqfwkye

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

ResearchGate publication ID

0 references

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