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Volumn 164, Issue 10, 2014, Pages 2672-2675

Copy number variation in bronchopulmonary dysplasia

Author keywords

[No Author keywords available]

Indexed keywords

ARTIFICIAL VENTILATION; BIRTH WEIGHT; CONTROLLED STUDY; COPY NUMBER VARIATION; GENE DELETION; GENE DUPLICATION; GENE FREQUENCY; GENETIC ASSOCIATION; GENOTYPE; HUMAN; INFANT; LETTER; LUNG DYSPLASIA; MAJOR CLINICAL STUDY; NEWBORN INTENSIVE CARE; PREDICTIVE VALUE; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; CASE CONTROL STUDY; GENETICS; NEWBORN;

EID: 84908230456     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36659     Document Type: Letter
Times cited : (15)

References (14)
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    • Parse CNV integrative copy number variation association software with quality tracking
    • Glessner JT, Li J, Hakonarson H. 2013. Parse CNV integrative copy number variation association software with quality tracking. Nucleic Acids Res 41: e64-e64.
    • (2013) Nucleic Acids Res , vol.41 , pp. e64-e64
    • Glessner, J.T.1    Li, J.2    Hakonarson, H.3
  • 6
    • 77950940258 scopus 로고    scopus 로고
    • The role of regional collaboratives: The California Perinatal Quality Care Collaborative Model
    • Gould JB. 2010. The role of regional collaboratives: The California Perinatal Quality Care Collaborative Model. Clin Perinatol 37:71-86.
    • (2010) Clin Perinatol , vol.37 , pp. 71-86
    • Gould, J.B.1
  • 7
    • 85007069160 scopus 로고    scopus 로고
    • Genome Studio Data Analysis Software [Whitepaper]
    • Illumina. 2011. Genome Studio Data Analysis Software [Whitepaper]. Retrieved from http://res.illumina.com/documents/products/datasheets/datasheet_genomestudio_software.pdf.
    • (2011)
  • 9
    • 51649115601 scopus 로고    scopus 로고
    • Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health
    • Lavoie PM, Pham C, Jang KL. 2008. Heritability of bronchopulmonary dysplasia, defined according to the consensus statement of the national institutes of health. Pediatrics 122:479-485.
    • (2008) Pediatrics , vol.122 , pp. 479-485
    • Lavoie, P.M.1    Pham, C.2    Jang, K.L.3
  • 13
    • 35948984173 scopus 로고    scopus 로고
    • Penn CNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
    • Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SFA, Hakonarson H, Bucan M. 2007. Penn CNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 17:1665-1674.
    • (2007) Genome Res , vol.17 , pp. 1665-1674
    • Wang, K.1    Li, M.2    Hadley, D.3    Liu, R.4    Glessner, J.5    Grant, S.F.A.6    Hakonarson, H.7    Bucan, M.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.