Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis.

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Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis.

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http://www.wikidata.org/entity/Q36635244

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2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Jacobsen Syndrome: Surgical Co ...... atients with Craniosynostosis.

@ast

Jacobsen Syndrome: Surgical Co ...... atients with Craniosynostosis.

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type

Item

label

Jacobsen Syndrome: Surgical Co ...... atients with Craniosynostosis.

@ast

Jacobsen Syndrome: Surgical Co ...... atients with Craniosynostosis.

@en

prefLabel

Jacobsen Syndrome: Surgical Co ...... atients with Craniosynostosis.

@ast

Jacobsen Syndrome: Surgical Co ...... atients with Craniosynostosis.

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P1476

Jacobsen Syndrome: Surgical Co ...... atients with Craniosynostosis.

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P2093

Adrian Perez Cabrera

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Etzalli P Linares Chávez

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Jaime Toral López

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Juan M Valdés Miranda

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Luz M González Huerta

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María Del Refugio Rivera Vega

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Olga M Messina Baas

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Sergio A Cuevas-Covarrubias

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P2860

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH

Hemorrhage, impaired hematopoiesis, and lethality in mouse embryos carrying a targeted disruption of the Fli1 transcription factor

FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia

The Ashwell receptor mitigates the lethal coagulopathy of sepsis

Identification of a Kir3.4 mutation in congenital long QT syndrome

Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)

Jacobsen syndrome.

Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).

Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay.

P304

229-235

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scholarly article

P356

10.1159/000442477

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P433

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P478

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P577

2015-12-18T00:00:00Z

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P698

26997943

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P921

craniosynostosis

P932

4772712

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