Related references
Note: Only part of the references are listed.Beckwith-Wiedemann syndrome
Rosanna Weksberg et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Parthenogenetic chimaerism/mosaicism with a Silver-Russell syndrome-like phenotype
K. Yamazawa et al.
JOURNAL OF MEDICAL GENETICS (2010)
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
Salah Azzi et al.
HUMAN MOLECULAR GENETICS (2009)
Molecular and clinical findings and their correlations in Silver-Russell syndrome:: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas
Kazuki Yamazawa et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2008)
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes
Masayo Kagami et al.
NATURE GENETICS (2008)
Placentomegaly in paternal uniparental disomy for human chromosome 14
M. Kagami et al.
PLACENTA (2008)
Androgenetic/Biparental Mosaicism in an Infant with Hepatic Mesenchymal Hamartoma and Placental Mesenchymal Dysplasia
Robyn C. Reed et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY (2008)
The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: Two new reports
Meredith Wilson et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Complex and segmental uniparental disomy updated
D. Kotzot
JOURNAL OF MEDICAL GENETICS (2008)
Disruption of parental-specific expression of imprinted genes in uniparental fetuses
Hidehiko Ogawa et al.
FEBS LETTERS (2006)
Limited evolutionary conservation of imprinting in the human placenta
D Monk et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Congenital hyperinsulinism and mosaic abnormalities of the ploidy
I Giurgea et al.
JOURNAL OF MEDICAL GENETICS (2006)
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia
KA Kaiser-Rogers et al.
JOURNAL OF MEDICAL GENETICS (2006)
Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese population
K Ikari et al.
JOURNAL OF HUMAN GENETICS (2001)