From Prenatal to Preimplantation Genetic Diagnosis of β-Thalassemia. Prevention Model in 8748 Cases: 40 Years of Single Center Experience

Re: ISUOG Practice Guidelines: invasive procedures for prenatal diagnosis

(2017) G. Monni et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma

(2016) Felix C.K. Wong et al.   Annual Review of Medicine

Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization

(2016) Daniel E. Sabath et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Single center experience in selective feticide in high-order multiple pregnancy: clinical and ethical issues

(2016) Giovanni Monni et al.   JOURNAL OF PERINATAL MEDICINE

Training for transabdominal villous sampling is feasible and safe

(2015) Giovanni Monni et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis

(2015) R. Akolekar et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies

(2014) Joanne Traeger-Synodinos et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

ESHRE Task Force on Ethics and Law22: Preimplantation Genetic Diagnosis

(2014) G. De Wert et al.   HUMAN REPRODUCTION

Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing

(2014) Li Xiong et al.   PRENATAL DIAGNOSIS

Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH

(2013) Ariane Blattner et al.   BLOOD CELLS MOLECULES AND DISEASES

Improved first-trimester aneuploidy risk assessment: an evolving challenge of training in invasive prenatal diagnosis

(2013) G. Monni et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

The Prevention of Thalassemia

(2013) A. Cao et al.   Cold Spring Harbor Perspectives in Medicine

The Molecular Basis of  -Thalassemia

(2013) S. L. Thein   Cold Spring Harbor Perspectives in Medicine

One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre

(2012) K. Haapaniemi Kouru et al.   HUMAN REPRODUCTION

New Perspectives on Embryo Biopsy: Not How, But When and Why?

(2012) Kangpu Xu et al.   SEMINARS IN REPRODUCTIVE MEDICINE

Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements

(2011) Marion Phylipsen et al.   HUMAN MUTATION

A Functional Element Necessary for Fetal Hemoglobin Silencing

(2011) Vijay G. Sankaran et al.   NEW ENGLAND JOURNAL OF MEDICINE

The inherited diseases of hemoglobin are an emerging global health burden

(2010) D. J. Weatherall   BLOOD

Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus

(2010) Y. M. D. Lo et al.   Science Translational Medicine

Microfluidics Digital PCR Reveals a Higher than Expected Fraction of Fetal DNA in Maternal Plasma

(2008) F. M. F. Lun et al.   CLINICAL CHEMISTRY

Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma

(2008) F. M. F. Lun et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA