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解雇規制緩和という『ブラック・スワン』に備えよ (日経BP)

担当 さて、令和初のコラムのネタなんですけど……どうしましょうね。ってか、センセーはあんまり令和とか、そういうの気にしないでしょうけど。 鈴木 いや、そういうの...

  1. POLO試験の結果は進行膵癌の診療を変え...
  2. 万年研修医の覚悟がないと時代に取り残され...
  3. 認知症の睡眠問題は「診立て」が肝心 (日...
  4. 再製造医療機器流通のために病院が注意すべ...

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「"Cheung SW "[Author]」の検索結果

452件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

Repeatability of choroidal thickness measurements with Spectralis OCT images.

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases.

Cortical-Basal Ganglia-Cerebellar Networks in Unilateral Vocal Fold Paralysis: A Pilot Study.

Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome.

Human caudate nucleus subdivisions in tinnitus modulation.

Role of corneal biomechanical properties in predicting of speed of myopic progression in children wearing orthokeratology lenses or single-vision spectacles.

Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

Cortical networks for speech motor control in unilateral vocal fold paralysis.

Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis.

Functional and Structural Brain Plasticity in Adult Onset Single-Sided Deafness.

Vocal motor control and central auditory impairments in unilateral vocal fold paralysis.

BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes.

Pre-treatment observation of axial elongation for evidence-based selection of children in Hong Kong for myopia control.

A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.

Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies.

Microarray analysis: first-trimester maternal serum free β-hCG and the risk of significant copy number variants.

Novel applications of array comparative genomic hybridization in molecular diagnostics.

Prenatal diagnosis of Wolf-Hirschhorn syndrome: from ultrasound findings, diagnostic technology to genetic counseling.

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