Suchergebnisse - "Li, Haoxian"

PubPharm (71)

61

Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)

enthalten in: Clinical chemistry | 2015

von Lv, W. | Wei, X. | Guo, R. | +10

62

Phenotype-genotype correlation analysis of 12 cases with Angelman/Prader-Willi syndrome

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2014

von Chen, C. | Peng, Y. | Xia, Y. | +5

63

Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity

enthalten in: Journal of genetics | 2014

von Mei, L. | Huang, Y. | Pan, Q. | +3

64

Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity

enthalten in: Journal of genetics | 2014

von MEI, L. | HUANG, Y. | PAN, Q. | +3

65

Identification of a novel SHOX mutation in a Chinese family with isolated Madelung deformity

enthalten in: Journal of genetics | 2014

von MEI, L. | HUANG, Y. | PAN, Q. | +3

66

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes

enthalten in: The Journal of molecular diagnostics : JMD | 2014

von Liang, D. | Peng, Y. | Lv, W. | +9

67

Copy Number Variation Sequencing for Comprehensive Diagnosis of Chromosome Disease Syndromes

enthalten in: The journal of molecular diagnostics | 2014

von Liang, D. | Peng, Y. | Lv, W. | +9

68

Phenotypic expansion of the interstitial 16p13.3 duplication : a case report and review of the literature

enthalten in: Gene | 2013

von Li, Z. | Liu, J. | Li, H. | +5

69

Phenotypic expansion of the interstitial 16p13.3 duplication: A case report and review of the literature

enthalten in: Gene | 2013

von Li, Z. | Liu, J. | Li, H. | +5

70

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

enthalten in: Prenatal diagnosis | 2013

von Liang, D. | Lv, W. | Wang, H. | +6