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Article

No evidence for increased prevalence of JAK2 V617F in women with a history of recurrent miscarriage.

British journal of haematology - 1 Mar 2009

Dahabreh Issa J, Jones Amy V, Voulgarelis Michael, Giannouli Stavroula, Zoi Christine, Alafakis-Tzannatos Christina, Varla-Leftherioti Marighoula, Moutsopoulos Haralampos M, Loukopoulos Dimitris, Fotiou Stelios, Cross Nicholas C P, Zoi Katerina

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19036091
DOI: 10.1111/j.1365-2141.2008.07510.x

Genes

JAK2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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No evidence for increased prevalence of JAK2 V617F in women with a history of recurrent miscarriage.PMID 19036091Read ↗

Recurrent spontaneous miscarriage is still a challenging diagnostic and therapeutic quagmire.Semantic proximity Read ↗

Testing for Inherited Thrombophilia in Recurrent MiscarriageSemantic proximity Read ↗

Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage.Semantic proximity Read ↗

Genetic Factors as a Cause of MiscarriageSemantic proximity Read ↗

Recurrent miscarriage II: clinical associations, causes, and managementSemantic proximity Read ↗

Recurrent miscarriage and thrombophiliaSemantic proximity Read ↗

Combined thrombophilic mutations in women with unexplained recurrent miscarriage.Semantic proximity Read ↗

Genetic thrombophilic mutations among couples with recurrent miscarriage.Semantic proximity Read ↗

Focus on recurrent miscarriage phenotypes.Semantic proximity Read ↗

Jak 2 Mutation In Recurrent Foetal Loss.Semantic proximity Read ↗

Recurrent miscarriageSemantic proximity Read ↗

Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.Semantic proximity Read ↗

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