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Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

Journal of medical genetics, 2003-01, Vol.40 (1), p.62-64

2003

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Large offspring syndrome: A bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann

Epigenetics, 2013-06, Vol.8 (6), p.591-601

2013

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Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith‐Wiedemann syndrome

Prenatal diagnosis, 2021-06, Vol.41 (7), p.798-816

2021

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(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome

Molecular genetics & genomic medicine, 2020-09, Vol.8 (9), p.e1386-n/a

2020

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Prenatal molecular testing and diagnosis of Beckwith‐Wiedemann syndrome

Prenatal diagnosis, 2021-06, Vol.41 (7), p.817-822

2021

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Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome

Cancers, 2022-11, Vol.14 (22), p.5563

2022

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Diagnosis and management of the phenotypic spectrum of twins with Beckwith‐Wiedemann syndrome

American journal of medical genetics. Part A, 2019-07, Vol.179 (7), p.1139-1147

2019

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CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Placenta (Eastbourne), 2009-06, Vol.30 (6), p.551-554

2009

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Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study

American journal of human genetics, 2004-09, Vol.75 (3), p.526-528

2004

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New genetic and clinical evidence associated with fetal Beckwith–Wiedemann syndrome

Prenatal diagnosis, 2021-06, Vol.41 (7), p.823-827

2021

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Prenatal features in Beckwith-Wiedemann syndrome and indications for prenatal testing

Journal of medical genetics, 2021-12, Vol.58 (12), p.842

2021

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Prenatal correction of IGF2 to rescue the growth phenotypes in mouse models of Beckwith-Wiedemann and Silver-Russell syndromes

Cell reports (Cambridge), 2021-02, Vol.34 (6), p.108729-108729, Article 108729

2021

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Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.877-880

2016

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Beckwith–Wiedemann Syndrome in Newborn of Mother with HELLP Syndrome/Preeclampsia: An Analysis of Literature and Case Report with Fetal Growth Restriction and Absence of CDKN1C Typical Pathogenic Genetic Variation

International journal of molecular sciences, 2023-09, Vol.24 (17), p.13360

2023

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Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications

American journal of medical genetics. Part A, 2022-05, Vol.188 (5), p.1562-1567

2022

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Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome

Prenatal diagnosis, 2015-04, Vol.35 (4), p.394-399

2015

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Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith–Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer

Taiwanese journal of obstetrics & gynecology, 2014-03, Vol.53 (1), p.90-94

2014

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Aberrant methylation of H19‐DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith–Wiedemann syndrome

American journal of medical genetics. Part A, 2012-07, Vol.158A (7), p.1670-1675

2012

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Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients

Fertility and sterility, 2005-02, Vol.83 (2), p.349-354

2005

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Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome

Journal of assisted reproduction and genetics, 2018-06, Vol.35 (6), p.985-992

2018

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Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

Epigenetics, 2015-07, Vol.10 (7), p.643-649

2015

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Fetal growth restriction in a genetic model of sporadic Beckwith-Wiedemann syndrome

Disease models & mechanisms, 2018-11, Vol.11 (11)

2018

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Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance

Clinical epigenetics, 2020-09, Vol.12 (1), p.139, Article 139

2020

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Hyperinsulinemic hypoglycemia in Beckwith–Wiedemann, Sotos, and Kabuki syndromes: A nationwide survey in Japan

American journal of medical genetics. Part A, 2017-02, Vol.173 (2), p.360-367

2017

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Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

Large offspring syndrome: A bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann

Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith‐Wiedemann syndrome

(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome

Prenatal molecular testing and diagnosis of Beckwith‐Wiedemann syndrome

Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome

Diagnosis and management of the phenotypic spectrum of twins with Beckwith‐Wiedemann syndrome

CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study

New genetic and clinical evidence associated with fetal Beckwith–Wiedemann syndrome

Prenatal features in Beckwith-Wiedemann syndrome and indications for prenatal testing

Prenatal correction of IGF2 to rescue the growth phenotypes in mouse models of Beckwith-Wiedemann and Silver-Russell syndromes

Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome

Beckwith–Wiedemann Syndrome in Newborn of Mother with HELLP Syndrome/Preeclampsia: An Analysis of Literature and Case Report with Fetal Growth Restriction and Absence of CDKN1C Typical Pathogenic Genetic Variation

Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications

Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome

Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring

Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith–Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer

Aberrant methylation of H19‐DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith–Wiedemann syndrome

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients

Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome

Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

Fetal growth restriction in a genetic model of sporadic Beckwith-Wiedemann syndrome

Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance

Hyperinsulinemic hypoglycemia in Beckwith–Wiedemann, Sotos, and Kabuki syndromes: A nationwide survey in Japan

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