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European guidelines for constitutional cytogenomic analysis

European journal of human genetics : EJHG, 2019-01, Vol.27 (1), p.1-16

2019

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Long-term effects of cognitive training on everyday functional outcomes in older adults

JAMA : the journal of the American Medical Association, 2006-12, Vol.296 (23), p.2805

2006

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Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data

Molecular cytogenetics, 2017-04, Vol.10 (1), p.12-12, Article 12

2017

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European guidelines for constitutional cytogenomic analysis

European journal of human genetics : EJHG, 2019-01, Vol.27 (1), p.1-16

2019

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QF-PCR: application, overview and review of the literature

Prenatal diagnosis, 2012-04, Vol.32 (4), p.309-314

2012

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Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance

Molecular cytogenetics, 2010-04, Vol.3 (1), p.9-9, Article 9

2010

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Multiplex ligation-dependent probe amplification using a completely synthetic probe set

BioTechniques, 2004-09, Vol.37 (3), p.399-405

2004

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Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre

BMC medical genetics, 2007-03, Vol.8 (1), p.9-9, Article 9

2007

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MLPA for confirmation of array CGH results and determination of inheritance

Molecular cytogenetics, 2010-10, Vol.3 (1), p.19-19

2010

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A novel non‐invasive prenatal sickle cell disease test for all at‐risk pregnancies

British journal of haematology, 2020-07, Vol.190 (1), p.119-124

2020

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Minimal Incision Protocols for Anesthesia, Pain Management, and Physical Therapy With Standard Incisions in Hip and Knee Arthroplasties

The Journal of arthroplasty, 2007, Vol.22 (1), p.20-25

2007

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Non-Invasive Prenatal Diagnosis (NIPD) of Sickle-Cell Disease By Massively Parallel Sequencing of Cell-Free Fetal DNA in Maternal Serum

Blood, 2019-11, Vol.134 (Supplement_1), p.2085-2085

2019

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Enhancing the quality of life of dementia caregivers from different ethnic or racial groups: a randomized, controlled trial

Annals of internal medicine, 2006-11, Vol.145 (10), p.727

2006

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Discrepancies between direct QF-PCR of chorionic villi and karyotype analysis of chorionic mesenchyme cells

Prenatal diagnosis, 2012-05, Vol.32 (5), p.501-502

2012

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A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report

Molecular cytogenetics, 2009-02, Vol.2 (1), p.9-9

2009

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Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis

Molecular cytogenetics, 2008-03, Vol.1 (1), p.2-2

2008

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Haematological chimerism masquerading as disorder of sex development

Clinical endocrinology (Oxford), 2020-05, Vol.92 (5), p.487-489

2020

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Quantitative fluorescence PCR analysis of >40000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X

Prenatal diagnosis, 2012-12, Vol.32 (12), p.1197

2012

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Recommended practice for laboratory reporting of non‐invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion

Prenatal diagnosis, 2017-07, Vol.37 (7), p.699-704

2017

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QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region

Prenatal diagnosis, 2010-06, Vol.30 (6), p.509-517

2010

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Collaborating for Safety in Amish Communities

Journal of agromedicine, 2014-04, Vol.19 (2), p.216-216

2014

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Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis: Gestation related laboratory failure rate in diagnostic amniocentesis

Prenatal diagnosis, 2016-08, Vol.36 (8), p.708-713

2016

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Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis

Prenatal diagnosis, 2016-08, Vol.36 (8), p.708-713

2016

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Combined QF-PCR and MLPA molecular analysis of miscarriage products: an efficient and robust alternative to karyotype analysis

Prenatal diagnosis, 2010-02, Vol.30 (2), p.133-137

2010

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Effect of memory impairment on training outcomes in ACTIVE

Journal of the International Neuropsychological Society, 2007-11, Vol.13 (6), p.953-960

2007

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European guidelines for constitutional cytogenomic analysis

Long-term effects of cognitive training on everyday functional outcomes in older adults

Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data

European guidelines for constitutional cytogenomic analysis

QF-PCR: application, overview and review of the literature

Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance

Multiplex ligation-dependent probe amplification using a completely synthetic probe set

Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre

MLPA for confirmation of array CGH results and determination of inheritance

A novel non‐invasive prenatal sickle cell disease test for all at‐risk pregnancies

Minimal Incision Protocols for Anesthesia, Pain Management, and Physical Therapy With Standard Incisions in Hip and Knee Arthroplasties

Non-Invasive Prenatal Diagnosis (NIPD) of Sickle-Cell Disease By Massively Parallel Sequencing of Cell-Free Fetal DNA in Maternal Serum

Enhancing the quality of life of dementia caregivers from different ethnic or racial groups: a randomized, controlled trial

Discrepancies between direct QF-PCR of chorionic villi and karyotype analysis of chorionic mesenchyme cells

A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report

Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis

Haematological chimerism masquerading as disorder of sex development

Quantitative fluorescence PCR analysis of >40000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X

Recommended practice for laboratory reporting of non‐invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion

QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region

Collaborating for Safety in Amish Communities

Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis: Gestation related laboratory failure rate in diagnostic amniocentesis

Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis

Combined QF-PCR and MLPA molecular analysis of miscarriage products: an efficient and robust alternative to karyotype analysis

Effect of memory impairment on training outcomes in ACTIVE

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