Protein C system defects in Indian children with thrombosis.

about

Coagulation disorders seen through the window of molecular biology.Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriers.Hypercoagulable State: Reply.Hyperbaric oxygen in treatment of neonatal arterial thromboembolism of lower extremities.

P2860

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P2860

Protein C system defects in Indian children with thrombosis.

Item

http://www.wikidata.org/entity/Q45078655

description

2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

@zh-hans

2004年学术文章

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2004年学术文章

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2004年學術文章

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2004年學術文章

@zh-hant

name

Protein C system defects in Indian children with thrombosis.

@en

Protein C system defects in Indian children with thrombosis.

@nl

type

Item

label

Protein C system defects in Indian children with thrombosis.

@en

Protein C system defects in Indian children with thrombosis.

@nl

prefLabel

Protein C system defects in Indian children with thrombosis.

@en

Protein C system defects in Indian children with thrombosis.

@nl

P1476

Protein C system defects in Indian children with thrombosis.

@en

P2093

Arijit Biswas

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M Kannan

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P K Gupta

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R Saxena

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Rafeeq P H Ahmed

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Veena Kalra

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85-88

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scholarly article

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10.1007/S00277-004-0952-X

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P433

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P478

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Maitreyee Bhattacharyya

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2004-09-23T00:00:00Z

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8266306

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P698

15449030

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P921

thrombosis

Protein C system defects in Indian children with thrombosis.

about

P2860

P2860

Protein C system defects in Indian children with thrombosis.

description

name

type

label

prefLabel

P1433

P1476

P2093

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

P356

P1433

P1476

P2093

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921