Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-beta (Q33347025)

26 July 2017

title

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

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26 July 2017

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Taichi Kato

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26 July 2017

Kazuki Kosaka

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26 July 2017

Misa Kimura

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26 July 2017

Shin-Ichiro Imamura

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26 July 2017

Osamu Yamada

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26 July 2017

Kazumasa Iwai

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26 July 2017

Masahiko Ando

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26 July 2017

Kunitaka Joh-o

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26 July 2017

Kenji Kuroe

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26 July 2017

Akira Ohtake

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26 July 2017

Atsuyoshi Takao

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26 July 2017

Kazuo Momma

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26 July 2017

Rumiko Matsuoka

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26 July 2017

language of work or name

English

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publication date

1 March 2003

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26 July 2017

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26 July 2017

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26 July 2017

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26 July 2017

page(s)

113-119

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A new concept of the cellular basis of immunity

26 July 2017

cites work

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Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

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Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

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Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

21 January 2018

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Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

21 January 2018

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Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

21 January 2018

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Velo-cardio-facial syndrome: a review of 120 patients.

21 January 2018

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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

21 January 2018

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Complementary DNA cloning of the alternatively expressed endothelial cell glycoprotein Ib beta (GPIb beta) and localization of the GPIb beta gene to chromosome 22

21 January 2018

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The 5' flanking region and chromosomal localization of the gene encoding human platelet membrane glycoprotein Ib alpha

21 January 2018

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A rapid method for starting a culture for the establishment of Epstein-Barr virus-transformed human lymphoblastoid cell lines

21 January 2018

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A monoclonal antibody to human platelet glycoprotein IIIa detects a related protein in cultured human endothelial cells

21 January 2018

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Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndrome

21 January 2018

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The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

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Structure and expression of the human septin gene HCDCREL-1

21 January 2018

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Reciprocal expression of infant- and adult-preferring transcripts of CDCrel-1 septin gene in the rat neocortex.

21 January 2018

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The septin CDCrel-1 binds syntaxin and inhibits exocytosis

21 January 2018

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Human platelet glycoprotein IX

21 January 2018

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Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility

21 January 2018

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A deletion in chromosome 22 can cause DiGeorge syndrome

21 January 2018

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

21 January 2018

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

21 January 2018

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Late‐Onset psychosis in the velo‐cardio‐facial syndrome

21 January 2018

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Duration of psychosis and outcome in first-episode schizophrenia

21 January 2018

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10.1097/01.GIM.0000056828.03164.30

21 January 2018

Identifiers

DOI

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26 July 2017

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