| (84) |
Designated Contracting States: |
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AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL
NO PL PT RO RS SE SI SK SM TR |
| (30) |
Priority: |
27.03.2013 GB 201305588
10.01.2014 GB 201400397
|
| (43) |
Date of publication of application: |
|
03.02.2016 Bulletin 2016/05 |
| (60) |
Divisional application: |
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19189461.7 |
| (73) |
Proprietor: BlueGnome Ltd |
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Cambridge, Cambridgeshire CB21 5XE (GB) |
|
| (72) |
Inventor: |
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- HANDYSIDE, Alan
Brighton
East Sussex BN2 9SA (GB)
|
| (74) |
Representative: Murgitroyd & Company |
|
Scotland House
165-169 Scotland Street
Glasgow G5 8PL
Glasgow G5 8PL (GB) |
| (56) |
References cited: :
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- D. CHRISTOPIKOU ET AL: "Polar body analysis by array comparative genomic hybridization
accurately predicts aneuploidies of maternal meiotic origin in cleavage stage embryos
of women of advanced maternal age", HUMAN REPRODUCTION, vol. 28, no. 5, 10 March 2013
(2013-03-10) , pages 1426-1434, XP055146306, ISSN: 0268-1161, DOI: 10.1093/humrep/det053
- ALAN H HANDYSIDE ET AL: "Multiple meiotic errors caused by predivision of chromatids
in women of advanced maternal age undergoing in vitro fertilisation", EUROPEAN JOURNAL
OF HUMAN GENETICS, vol. 20, no. 7, 1 July 2012 (2012-07-01), pages 742-747, XP055146383,
ISSN: 1018-4813, DOI: 10.1038/ejhg.2011.272
- ALAN H. HANDYSIDE: "Molecular origin of female meiotic aneuploidies", BIOCHIMICA ET
BIOPHYSICA ACTA (BBA) - MOLECULAR BASIS OF DISEASE, vol. 1822, no. 12, 1 December
2012 (2012-12-01), pages 1913-1920, XP055146382, ISSN: 0925-4439, DOI: 10.1016/j.bbadis.2012.07.007
- ALTARESCU G ET AL: "Gene location matters: polar body analysis has limited informativity
in centromeric genes", REPRODUCTIVE BIOMEDICINE ONLINE, REPRODUCTIVE HEALTHCARE LTD,
GB, vol. 18, 1 January 2009 (2009-01-01), pages S-10, XP027051939, ISSN: 1472-6483
[retrieved on 2009-01-01]
- A. H. HANDYSIDE ET AL: "Karyomapping: a universal method for genome wide analysis
of genetic disease based on mapping crossovers between parental haplotypes", JOURNAL
OF MEDICAL GENETICS, vol. 47, no. 10, 25 October 2009 (2009-10-25), pages 651-658,
XP055146321, ISSN: 0022-2593, DOI: 10.1136/jmg.2009.069971
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