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An economic analysis of preimplantation genetic testing for aneuploidy by polar body biopsy in advanced maternal age

BJOG : an international journal of obstetrics and gynaecology, 2020-05, Vol.127 (6), p.710-718

2020

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Prenatal and preimplantation diagnosis of hemoglobinopathies

International journal of laboratory hematology, 2018-05, Vol.40 (S1), p.74-82

2018

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ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011

Human reproduction (Oxford), 2015-08, Vol.30 (8), p.1763-1789

2015

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Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion

American journal of medical genetics. Part A, 2024-07, p.e63826

2024

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The ESHRE PGD Consortium: 10 years of data collection

Human reproduction update, 2012-05, Vol.18 (3), p.234-247

2012

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Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

Human reproduction (Oxford), 2023-12, Vol.38 (12), p.2526-2535

2023

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Preimplantation genetic diagnosis, an alternative to conventional prenatal diagnosis of the hemoglobinopathies

International journal of laboratory hematology, 2013-12, Vol.35 (6), p.571-579

Traeger-Synodinos, J.

2013

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ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010

Human reproduction (Oxford), 2014-05, Vol.29 (5), p.880-903

2014

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ESHRE PGD consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008

Human reproduction (Oxford), 2010-11, Vol.25 (11), p.2685-2707

2010

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ESHRE PGD Consortium data collection IX: cycles from January to December 2006 with pregnancy follow-up to October 2007

Human reproduction (Oxford), 2009-08, Vol.24 (8), p.1786-1810

2009

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The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study

Human reproduction (Oxford), 2018-03, Vol.33 (3), p.520-530

2018

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ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006

Human reproduction (Oxford), 2008-12, Vol.23 (12), p.2629-2645

2008

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Diagnosis and molecular characterization of a novel α 0 -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.e124

2017

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Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD)

Journal of cystic fibrosis, 2016-03, Vol.15 (2), p.163-170

2016

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Scanning of β‐globin gene for identification of β‐thalassemia mutation in Romanian population

Journal of cellular and molecular medicine, 2004-04, Vol.8 (2), p.232-240

2004

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Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

Obstetrical & gynecological survey, 2024-03, Vol.79 (3), p.164-165

2024

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PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol

Reproductive biomedicine online, 2009, Vol.19 (3), p.418-425

2009

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Diagnosis and molecular characterization of a novel [alpha]0-thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.e124

2017

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Diagnosis and molecular characterization of a novel α0‐thalassemia deletion (–Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.e124-e126

2017

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Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome

European journal of paediatric neurology, 2007-07, Vol.11 (4), p.235-239

2007

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Two novel variants in theTCF12gene identified in cases with craniosynostosis

Application of clinical genetics, 2019-02, Vol.12, p.19-25

2019

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Genotyping of Single-Nucleotide Polymorphisms by Primer Extension Reaction in a Dry-Reagent Dipstick Format

Analytical chemistry (Washington), 2007-01, Vol.79 (2), p.395-402

2007

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Molecular Basis of α-thalassaemia

Thalassemia reports, 2011-12, Vol.1 (12), p.e13

Traeger-Synodinos, J.

2011

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ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening

Human reproduction (Oxford), 2012-08, Vol.27 (8), p.2569-2569

2012

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An economic analysis of preimplantation genetic testing for aneuploidy by polar body biopsy in advanced maternal age

Prenatal and preimplantation diagnosis of hemoglobinopathies

ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011

Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion

The ESHRE PGD Consortium: 10 years of data collection

Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

Preimplantation genetic diagnosis, an alternative to conventional prenatal diagnosis of the hemoglobinopathies

ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010

ESHRE PGD consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008

ESHRE PGD Consortium data collection IX: cycles from January to December 2006 with pregnancy follow-up to October 2007

The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study

ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006

P135: THE CLINGEN HEMOGLOBINOPATHY VARIANT CURATION EXPERT PANEL

Diagnosis and molecular characterization of a novel α 0 -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD)

Scanning of β‐globin gene for identification of β‐thalassemia mutation in Romanian population

Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol

Diagnosis and molecular characterization of a novel [alpha]0-thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Diagnosis and molecular characterization of a novel α0‐thalassemia deletion (–Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome

Two novel variants in theTCF12gene identified in cases with craniosynostosis

Genotyping of Single-Nucleotide Polymorphisms by Primer Extension Reaction in a Dry-Reagent Dipstick Format

Molecular Basis of α-thalassaemia

ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening

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