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Molecular Characterization of a Rare Case of Monozygotic Dichorionic Diamniotic Twin Pregnancy after Single Blastocyst Transfer in Preimplantation Genetic Testing (PGT)

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10835

2022

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UV/Vis Characterization and Fate of Organic Amendment Fractions in a Dune Soil in Dakar, Senegal

Pedosphere, 2015-06, Vol.25 (3), p.372-385

2015

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Efficient strategies for preimplantation genetic diagnosis of spinal muscular atrophy

Fertility and sterility, 2008-08, Vol.90 (2), p.443.e7-443.e12

2008

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Large genomic rearrangements in the CFTR gene contribute to CBAVD

BMC medical genetics, 2007-04, Vol.8 (1), p.22-22

2007

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Evolution of post–pulmonary vein isolation atrial fibrillation inducibility at redo ablation: Electrophysiological evidence of extra–pulmonary vein substrate progression

Heart rhythm, 2019-08, Vol.16 (8), p.1160-1166

2019

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Are ovarian response and pregnancy rates similar in selected FMR1 premutated and mutated patients undergoing preimplantation genetic testing?

Journal of assisted reproduction and genetics, 2020-07, Vol.37 (7), p.1675-1683

2020

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Cervical cancer screening in low-resource settings: a smartphone image application as an alternative to colposcopy

International journal of women's health, 2017-01, Vol.9, p.455-461

2017

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Germline mosaicism is a pitfall in PGD for X‐linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal origin

Prenatal diagnosis, 2017-02, Vol.37 (2), p.201-205

2017

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The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus

European journal of human genetics : EJHG, 2016-04, Vol.24 (4), p.469-478

2016

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Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital service

Reproductive biomedicine online, 2018-02, Vol.36 (2), p.154-163

2018

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Germline mosaicism is a pitfall in PGD for X-linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal origin: Parental origin of gonadal mosaicism reassessed by single sperm typing

Prenatal diagnosis, 2017-02, Vol.37 (2), p.201-205

2017

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A Broad Test Based on Fluorescent-Multiplex PCR for Noninvasive Prenatal Diagnosis of Cystic Fibrosis

Fetal diagnosis and therapy, 2019-06, Vol.45 (6), p.403-412

2019

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Dispersion of natural arsenic in the Malcantone watershed, Southern Switzerland: field evidence for repeated sorption–desorption and oxidation–reduction processes

Geoderma, 2004-10, Vol.122 (2), p.205-234

2004

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New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?

European journal of human genetics : EJHG, 2010-05, Vol.18 (5), p.533-538

2010

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Efficiency of Primed In Situ Labeling (PRINS) Method for Interphasic Chromosomal Screening: a Review

ACTA HISTOCHEMICA ET CYTOCHEMICA, 1998, Vol.31(5), pp.369-374

1998

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Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene

Reproductive biomedicine online, 2005-04, Vol.10 (4), p.519-526

2005

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Short Communication: Rapid detection of the [Delta]F508 mutation in single cells using DHPLC: Implications for preimplantation genetic diagnosis

Journal of assisted reproduction and genetics, 2003-04, Vol.20 (4), p.153

2003

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Short Communication: Rapid Detection of the ΔF508 Mutation in Single Cells Using DHPLC: Implications for Preimplantation Genetic Diagnosis

Journal of assisted reproduction and genetics, 2003-04, Vol.20 (4), p.153-156

2003

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Large genomic rearrangements in the CFTRgene contribute to CBAVD

BMC medical genetics, 2007-04, Vol.8 (1), Article 22

2007

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Assessment of aneuploidy for chromosomes 8,9,13,16, and 21 in human sperm by using primed in situ labeling technique

American journal of human genetics, 1996-04, Vol.58 (4), p.797-802

1996

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Rapid detection of the ΔF508 mutation in single cells using DHPLC: Implications for preimplantation genetic diagnosis

Journal of assisted reproduction and genetics, 2003-04, Vol.20 (4), p.153-156

2003

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Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation

Journal of medical genetics, 2001-01, Vol.38 (1), p.67-73

2001

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Evidence of Somatic and Germinal Mosaicism in Pseudo–Low-Penetrant Hereditary Retinoblastoma, by Constitutional and Single-Sperm Mutation Analysis

American journal of human genetics, 1998-12, Vol.63 (6), p.1903-1907

1998

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Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family

Human genetics, 1998-12, Vol.103 (6), p.658-661

1998

Volltextzugriff (PDF)

Molecular Characterization of a Rare Case of Monozygotic Dichorionic Diamniotic Twin Pregnancy after Single Blastocyst Transfer in Preimplantation Genetic Testing (PGT)

International journal of molecular sciences, 2022, Vol.23 (18)

2022

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Molecular Characterization of a Rare Case of Monozygotic Dichorionic Diamniotic Twin Pregnancy after Single Blastocyst Transfer in Preimplantation Genetic Testing (PGT)

UV/Vis Characterization and Fate of Organic Amendment Fractions in a Dune Soil in Dakar, Senegal

Efficient strategies for preimplantation genetic diagnosis of spinal muscular atrophy

Large genomic rearrangements in the CFTR gene contribute to CBAVD

Evolution of post–pulmonary vein isolation atrial fibrillation inducibility at redo ablation: Electrophysiological evidence of extra–pulmonary vein substrate progression

Are ovarian response and pregnancy rates similar in selected FMR1 premutated and mutated patients undergoing preimplantation genetic testing?

Cervical cancer screening in low-resource settings: a smartphone image application as an alternative to colposcopy

Germline mosaicism is a pitfall in PGD for X‐linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal origin

The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus

Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital service

Germline mosaicism is a pitfall in PGD for X-linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal origin: Parental origin of gonadal mosaicism reassessed by single sperm typing

A Broad Test Based on Fluorescent-Multiplex PCR for Noninvasive Prenatal Diagnosis of Cystic Fibrosis

Dispersion of natural arsenic in the Malcantone watershed, Southern Switzerland: field evidence for repeated sorption–desorption and oxidation–reduction processes

New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?

Efficiency of Primed In Situ Labeling (PRINS) Method for Interphasic Chromosomal Screening: a Review

Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene

Short Communication: Rapid detection of the [Delta]F508 mutation in single cells using DHPLC: Implications for preimplantation genetic diagnosis

Short Communication: Rapid Detection of the ΔF508 Mutation in Single Cells Using DHPLC: Implications for Preimplantation Genetic Diagnosis

Large genomic rearrangements in the CFTRgene contribute to CBAVD

Assessment of aneuploidy for chromosomes 8,9,13,16, and 21 in human sperm by using primed in situ labeling technique

Rapid detection of the ΔF508 mutation in single cells using DHPLC: Implications for preimplantation genetic diagnosis

Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation

Evidence of Somatic and Germinal Mosaicism in Pseudo–Low-Penetrant Hereditary Retinoblastoma, by Constitutional and Single-Sperm Mutation Analysis

Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family

Molecular Characterization of a Rare Case of Monozygotic Dichorionic Diamniotic Twin Pregnancy after Single Blastocyst Transfer in Preimplantation Genetic Testing (PGT)

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