(Q33405083)

26 July 2017

0 references

Hematological abnormalities and 22q11.2 deletion syndrome (English)

1 reference

26 July 2017

Rafael Fabiano Machado Rosa

1

1 reference

26 July 2017

Rosana Cardoso Manique Rosa

2

1 reference

26 July 2017

Pedro Paulo Albino Dos Santos

3

1 reference

26 July 2017

Paulo Ricardo Gazzola Zen

4

1 reference

26 July 2017

Giorgio Adriano Paskulin

5

1 reference

26 July 2017

1 January 2011

1 reference

Revista brasileira de hematologia e hemoterapia

26 July 2017

1 reference

26 July 2017

33

1 reference

26 July 2017

2

1 reference

26 July 2017

151-154

1 reference

Chromosome 22q11.2 deletion presenting with immune-mediated cytopenias, macrothrombocytopenia and platelet dysfunction

26 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Frequency of thrombocytopenia and large platelets correlates neither with conotruncal cardiac anomalies nor immunological features in the chromosome 22q11.2 deletion syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Hematological abnormalities in a patient with a 22q11.2 deletion

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-beta

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Evans syndrome in a patient with chromosome 22q11.2 deletion syndrome: a case report

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Bernard-Soulier syndrome associated with 22q11.2 microdeletion

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Recurrent immune cytopenias in two patients with DiGeorge/velocardiofacial syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Heterozygous loss of platelet glycoprotein (GP) Ib-V-IX variably affects platelet function in velocardiofacial syndrome (VCFS) patients.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3520641

Predicting 22q11.2 deletion syndrome: a novel method using the routine full blood count

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23284264

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/velo-cardio-facial chromosomal region in 22q11.2.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23284264

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Velocardiofacial syndrome patients with a heterozygous chromosome 22q11 deletion have giant platelets

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23284264

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.5581/1516-8484.20110037

1 reference

26 July 2017

1 reference

26 July 2017

1 reference