Brain hemorrhages in Jacobsen syndrome: A retrospective review of six cases and clinical recommendations.

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Brain hemorrhages in Jacobsen syndrome: A retrospective review of six cases and clinical recommendations.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Brain hemorrhages in Jacobsen ...... and clinical recommendations.

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Brain hemorrhages in Jacobsen ...... and clinical recommendations.

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Brain hemorrhages in Jacobsen ...... and clinical recommendations.

@en

Brain hemorrhages in Jacobsen ...... and clinical recommendations.

@nl

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Brain hemorrhages in Jacobsen ...... and clinical recommendations.

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Brain hemorrhages in Jacobsen ...... and clinical recommendations.

@nl

P1476

Brain hemorrhages in Jacobsen ...... and clinical recommendations.

@en

P2093

Paul Grossfeld

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P2860

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

PX-RICS-deficient mice mimic autism spectrum disorder in Jacobsen syndrome through impaired GABAA receptor trafficking

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.

Evidence for autism spectrum disorder in Jacobsen syndrome: identification of a candidate gene in distal 11q.

Jacobsen syndrome: Advances in our knowledge of phenotype and genotype.

The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency.

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.

Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder.

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667-670

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scholarly article

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10.1002/AJMG.A.38032

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English

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173

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2017-03-01T00:00:00Z

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28211970

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