Arama Sonuçları - "phenotyping"
Önerilen Konular
Önerilen Konular
- Biology, life sciences 97
- Research & information: general 90
- Medicine 80
- Neurosciences 20
- Genetics (non-medical) 18
- Botany & plant sciences 17
- Technology, engineering, agriculture 15
- History of engineering & technology 13
- Food & society 12
- Microbiology (non-medical) 12
- Oncology 11
- Science: general issues 11
- Medical genetics 10
- Technology: general issues 10
- Immunology 9
- Agricultural science 8
- Pharmacology 8
- Neurology & clinical neurophysiology 7
- Plant physiology 7
- Agronomy & crop production 6
- Evolution 6
- Plant reproduction & propagation 6
- Sustainable agriculture 6
- Agriculture 5
- Environmental science, engineering & technology 5
- Physiology 5
- Public health & preventive medicine 5
- Analytical chemistry 4
- Biochemistry 4
- Ecological science, the Biosphere 4
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481
A comprehensive genotype-phenotype evaluation of eight Chinese probands with Waardenburg syndrome
Baskı/Yayın Bilgisi 2022Connect to this object online.
Kitap -
482
Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn
Baskı/Yayın Bilgisi 2020Connect to this object online.
Kitap -
483
Sleep duration and metabolic body size phenotypes among Chinese young workers
Baskı/Yayın Bilgisi 2022Connect to this object online.
Kitap -
484
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485
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486
Identification of a novel PHGDH covalent inhibitor by chemical proteomics and phenotypic profiling
Baskı/Yayın Bilgisi 2022Connect to this object online.
Kitap -
487
Contribution of neural cell death to depressive phenotypes of streptozotocin-induced diabetic mice
Baskı/Yayın Bilgisi 2014Connect to this object online.
Kitap -
488
Dual Tumor Suppressor and Tumor Promoter Action of Sirtuins in Determining Malignant Phenotype
Baskı/Yayın Bilgisi 2019Connect to this object online.
Kitap -
489
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490
Clinical Features and Insulin Resistance in Men with a Metabolically Unhealthy Obesity Phenotype
Baskı/Yayın Bilgisi 2020Connect to this object online.
Kitap -
491
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492
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493
A rare case of complete uniparental isodisomy of chromosome 2 with no phenotypic abnormalities
Baskı/Yayın Bilgisi 2021Connect to this object online.
Kitap -
494
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495
Case Report: Expanded delineation of phenotype of TRPM3-related neurodevelopmental disorders
Baskı/Yayın Bilgisi 2024Connect to this object online.
Kitap -
496
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497
Genotypic and phenotypic heterogeneity among Chinese pediatric genetic white matter disorders
Baskı/Yayın Bilgisi 2023Connect to this object online.
Kitap -
498
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499
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500