Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith–Wiedemann syndrome and Silver–Russell syndrome

Maternally transmitted foetal H19 variants and associations with birth weight

(2011) Clive J. Petry et al.   HUMAN GENETICS

Methylation profiling in individuals with Russell-Silver syndrome

(2010) Maria S. Peñaherrera et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Russell-Silver syndrome

(2010) Thomas Eggermann   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Beckwith-Wiedemann syndrome

(2010) Sanaa Choufani et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders

(2010) DK Bourque et al.   CLINICAL GENETICS

Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseases

(2010) Salah Azzi et al.   Epigenetics

Epigenotype-phenotype correlations in Silver-Russell syndrome

(2010) E. L. Wakeling et al.   JOURNAL OF MEDICAL GENETICS

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

(2009) Salah Azzi et al.   HUMAN MOLECULAR GENETICS

Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome)

(2009) Esther Meyer et al.   PLoS Genetics

Continuous growth reference from 24thweek of gestation to 24 months by gender

(2008) Aimon Niklasson et al.   BMC Pediatrics

Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae

(2008) Lin Guo et al.   DEVELOPMENTAL BIOLOGY

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome

(2008) Jet Bliek et al.   EUROPEAN JOURNAL OF HUMAN GENETICS