(Q37215159)

19 August 2017

0 references

Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q- syndrome (English)

1 reference

19 August 2017

1 reference

1

Adrianna Vlachos

1 reference

19 August 2017

Jason E Farrar

2

1 reference

19 August 2017

Eva Atsidaftos

3

1 reference

19 August 2017

Ellen Muir

4

1 reference

19 August 2017

Anupama Narla

5

1 reference

19 August 2017

Thomas C Markello

6

1 reference

19 August 2017

Sharon A Singh

7

1 reference

19 August 2017

Michael Landowski

8

1 reference

19 August 2017

Hanna T Gazda

9

1 reference

19 August 2017

Lionel Blanc

10

1 reference

19 August 2017

Johnson M Liu

11

1 reference

19 August 2017

Steven R Ellis

12

1 reference

19 August 2017

Robert J Arceci

13

1 reference

19 August 2017

Benjamin L Ebert

14

1 reference

19 August 2017

David M Bodine

15

1 reference

19 August 2017

Jeffrey M Lipton

16

1 reference

19 August 2017

language of work or name

English

0 references

publication date

13 August 2013

1 reference

19 August 2017

4

1 reference

based on heuristic

inferred from page(s)

published in

Blood

1 reference

19 August 2017

122

1 reference

19 August 2017

14

1 reference

19 August 2017

2487-2490

1 reference

Clinical utility gene card for: Diamond-Blackfan anemia--update 2013.

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Sensitive quantification of mosaicism using high density SNP arrays and the cumulative distribution function

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Ribosomal protein gene deletions in Diamond-Blackfan anemia.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

A critical role for phosphatase haplodeficiency in the selective suppression of deletion 5q MDS by lenalidomide

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Efficacy of lenalidomide in myelodysplastic syndromes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Elevated red cell adenosine deaminase activity: a marker of disordered erythropoiesis in Diamond-Blackfan anaemia and other haematologic diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Extensive gene deletions in Japanese patients with Diamond-Blackfan anemia

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790513

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23943650

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/23943650

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1182/BLOOD-2013-06-509935

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

23943650

1 reference