Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques

A novel large deletion of the ICR1 region including H19 and putative enhancer elements

(2015) Helen Fryssira et al.   BMC Medical Genetics

(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome

(2015) Alessandro Mussa et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Increased risk of congenital heart disease in twins in the North of England between 1998 and 2010

(2015) K E Best et al.   HEART

Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse

(2015) Tomas Babak et al.   NATURE GENETICS

High Frequency of Imprinted Methylation Errors in Human Preimplantation Embryos

(2015) Carlee R. White et al.   Scientific Reports

Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment

(2014) F. Court et al.   GENOME RESEARCH

Epigenetic germline mosaicism in infertile men

(2014) Sandra Laurentino et al.   HUMAN MOLECULAR GENETICS

A New Overgrowth Syndrome is due to Mutations inRNF125

(2014) Jair Tenorio et al.   HUMAN MUTATION

Complex Tissue-Specific Epigenotypes in Russell-Silver Syndrome Associated with 11p15 ICR1 Hypomethylation

(2014) Salah Azzi et al.   HUMAN MUTATION

Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing

(2014) Thomas Eggermann et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects

(2014) Abdulla Ibrahim et al.   Clinical Epigenetics

Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance

(2013) F. Brioude et al.   Hormone Research in Paediatrics

Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology

(2013) Louise Tee et al.   Clinical Epigenetics

Imprinted DNA methylation reprogramming during early mouse embryogenesis at theGpr1-Zdbf2locus is linked to longcis-intergenic transcription

(2012) Hisato Kobayashi et al.   FEBS LETTERS

Adults with Sotos syndrome: Review of 21 adults with molecularly confirmed NSD1 alterations, including a detailed case report of the oldest person

(2011) Matthew R. Fickie et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Macroglossia and Beckwith-Wiedemann syndrome

(2011) Dragan Krasic et al.   Srpski Arhiv za Celokupno Lekarstvo

De novo DNA methylation: a germ cell perspective

(2011) Sébastien A. Smallwood et al.   TRENDS IN GENETICS

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies

(2008) D. Lim et al.   HUMAN REPRODUCTION