Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A novel JAK2 splicing mutation in neonatal myeloproliferative disorder accompanying congenital anomalies.

British journal of haematology - 1 Jun 2009

Ohnishi Hiroaki, Hosoi Ken-ichirou, Yoshino Hiroshi, Sugiura Masatoshi, Matsushima Satsuki, Watanabe Takashi, Bessho Fumio

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital Abnormalities
Share to JAK2 gene
Share to Infant, Low Birth Weight
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Isoenzymes

Share to Janus Kinase 2

Share to Mutation

Share to Myeloproliferative Disorders

Source

Identifiers

PMID: 19344419
DOI: 10.1111/j.1365-2141.2009.07672.x

Genes

JAK2

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel JAK2 splicing mutation in neonatal myeloproliferative disorder accompanying congenital anomalies.PMID 19344419Read ↗

A JAK2 mutation in myeloproliferative disorders: pathogenesis and therapeutic and scientific prospectsSemantic proximity Read ↗

C-kit activating mutation in a neonate with in-utero presentation of systemic mastocytosis associated with myeloproliferative disorder.Semantic proximity Read ↗

Germline JAK2 L611S mutation in a child with thrombocytosis.Semantic proximity Read ↗

Mutations in GATA2 are rare in juvenile myelomonocytic leukemia.Semantic proximity Read ↗

JAK2 V617F: a single mutation in the myeloproliferative group of disorders.Semantic proximity Read ↗

[JAK2 mutation in myeloproliferative disorders].Semantic proximity Read ↗

Molecular defects in chronic myeloproliferative disorders.Semantic proximity Read ↗

<i>JAK2</i>Mutations in Myeloproliferative DisordersSemantic proximity Read ↗

[Pathogenetic role of JAK2 gene mutation in chronic myeloproliferative disorders].Semantic proximity Read ↗

Update on the impact of the JAK2 mutation on signalling pathways in myeloproliferative disorders.Semantic proximity Read ↗

A neonate diagnosed with Noonan syndrome with myeloproliferative change.Semantic proximity Read ↗

In Response to: Pediatric Myelodysplastic Syndrome with Germline RRAS Mutation: Expanding the Phenotype of RASopathies.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.