Zobrazeno 1 - 4
of 4
pro vyhledávání: '"F S, Togneri"'
Autor:
Nicholas D. James, Ronald J. Wapner, Dominic J. McMullan, Mark D. Kilby, C. H. Meller, Eamonn R. Maher, SC Hillman, E. J. Maher, G Hall, David S. Williams, F. S. Togneri
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 41:610-620
Objectives Chromosomal microarray analysis (CMA) is utilized in prenatal diagnosis to detect chromosomal abnormalities not visible by conventional karyotyping. A prospective cohort of women undergoing fetal CMA and karyotyping following abnormal pren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b533c06a7dbd34841da7391860e3d510
https://doi.org/10.1002/uog.12464
https://doi.org/10.1002/uog.12464
Autor:
S C, Hillman, D J, McMullan, G, Hall, F S, Togneri, N, James, E J, Maher, C H, Meller, D, Williams, R J, Wapner, E R, Maher, M D, Kilby
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 41(6)
Chromosomal microarray analysis (CMA) is utilized in prenatal diagnosis to detect chromosomal abnormalities not visible by conventional karyotyping. A prospective cohort of women undergoing fetal CMA and karyotyping following abnormal prenatal ultras
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f62598829b96912b7c141be8f7c5fe39
https://pubmed.ncbi.nlm.nih.gov/24591235
https://pubmed.ncbi.nlm.nih.gov/24591235
Autor:
E. J. Maher, Dominic J. McMullan, César Meller, Kilby, Ronald J. Wapner, F. S. Togneri, G Hall, David S. Williams, Eamonn R. Maher, SC Hillman, Nicholas D. James
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 98:A4.3-A5
Background Chromosomal microarray testing (CMA) is utilised in prenatal diagnosis to detect chromosomal abnormalities not visible by full, conventional karyotyping. We present our prospective cohort of women undergoing fetal microarray and karyotypin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77a8e258558c4c0c636a8e2f86d19b76
https://doi.org/10.1136/archdischild-2013-303966.013
https://doi.org/10.1136/archdischild-2013-303966.013
Autor:
V E Davison, SC Hillman, Dominic J. McMullan, Mark D. Kilby, F. S. Togneri, R Maher, G Hall, David S. Williams, L Cooper-Charles
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 96:Fa12-Fa12
Background Array comparative genomic hybridisation (aCGH) technology has allowed examination of the human genome at previously unthinkable resolution. It has enabled the detection of microdeletions and microduplications too small to be noted on stand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38271f62f825de459c383c067f77d094
https://doi.org/10.1136/adc.2011.300160.37
https://doi.org/10.1136/adc.2011.300160.37