Congenital macrothrombocytopenia is a heterogeneous disorder in India. - Wikidata - wikimedia - TriplyDB

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

http://www.wikidata.org/entity/Q33432986

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Congenital macrothrombocytopenia is a heterogeneous disorder in India.

http://www.wikidata.org/entity/Q33432986

description

2016 nî lūn-bûn

@nan

2016 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2016年の論文

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2016年論文

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2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

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2016年論文

@zh-tw

2016年论文

@wuu

name

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

@ast

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

@en

type

label

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

@ast

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

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prefLabel

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

@ast

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

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Congenital macrothrombocytopenia is a heterogeneous disorder in India.

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D J Hampshire

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K Ghosh

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L Mukherjee

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M E Daly

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M Ghosh

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Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure.

Prediction of missense mutation functionality depends on both the algorithm and sequence alignment employed

Macrothrombocytopenia in north India: role of automated platelet data in the detection of an under diagnosed entity.

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome.

Role of antiidiotypic antibodies on the clinical course of idiopathic thrombocytopenic purpura.

Stomatocytic haemolysis and macrothrombocytopenia (Mediterranean stomatocytosis/macrothrombocytopenia) is the haematological presentation of phytosterolaemia.

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias.

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)

R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura.

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10.1111/HAE.12917

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4

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22

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Maitreyee Bhattacharyya

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2016-06-13T00:00:00Z

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27291889

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Giant platelet disorder