Results 131 to 140 of about 14,149 (242)

Phenotype, cancer risk, and surveillance in Beckwith–Wiedemann syndrome depending on molecular genetic subgroups

American Journal of Medical Genetics. Part A, 2016
S. Maas, F. Vansenne, D. Kadouch, A. Ibrahim, J. Bliek, Saskia M. J. Hopman, M. Mannens, J. Merks, E. Maher, R. Hennekam   +9 more
semanticscholar   +1 more source

Effects of Alcohol on the Regulation of Imprinted Genes in Mouse Stem Cells [PDF]

, 2013
Effects of Alcohol on the Regulation of Imprinted Genes in Mouse Stem Cells. (December 2013) Alyssa Crocker Department of Animal Science Texas A&M University Research Advisor: Dr. Michael Golding Department of Veterinary Physiology and Pharmacology
Crocker, Alyssa
core   +1 more source

Beckwith-Wiedemann Syndrome Revisited [PDF]

Human Mutation, 2015
openaire   +2 more sources

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

Journal of Medical Genetics, 2003
Eamonn R. Maher, L. Brueton, S. Bowdin, A. Luharia, W. Cooper, T. Cole, F. Macdonald, J. Sampson, C. Barratt, W. Reik, M. M. Hawkins   +10 more
semanticscholar   +1 more source

Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome

Pediatrics, 2017
A. Mussa, C. Molinatto, F. Cerrato, O. Palumbo, M. Carella, G. Baldassarre, D. Carli, C. Peris, A. Riccio, G. Ferrero   +9 more
semanticscholar   +1 more source

Adrenal masses associated with Beckwith Wiedemann syndrome in the newborn

African Journal of Paediatric Surgery, 2010
Adrenal cystic lesions are rare and may be associated with both complete and incomplete Beckwith syndrome (BWS). Because the adrenal gland often houses malignant lesions, differentiation between benign and malignant lesions of the gland, although usually
Taide Devendra, Bendre Pradnya, Redkar Rajeev, Hambarde Sandeep   +3 more
doaj  

Registro nazionale malattie rare. Epidemiologia di 44 malformazioni congenite rare in Italia [PDF]

The main purpose of this report is to provide health operators and the scientific community with information about the epidemiology of some Rare Congenital Malformations (RCMs). Statistical analysis was carried out on data of selected RCMs, detected both
Bianchi, Fabrizio, Minichilli, Fabrizio, Pierini, Anna, Salerno, Paolo, Taruscio, Domenica   +4 more
core  

Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances. [PDF]

Clin Epigenetics
Cecere F, Pignata L, D'Angelo E, Giaccari C, Saadat A, Sparago A, Angelini C, Hay Mele B, Mussa A, Ferrero GB, Scarano G, Gori G, Di Maria E, Romano C, Tarani L, Piscopo C, Scala I, Tenorio JA, Lapunzina P, Cerrato F, Riccio A.   +20 more
europepmc   +2 more sources

Introduction to the Beckwith-Wiedemann Syndrome and Cancer Special Issue. [PDF]

Cancers (Basel), 2023
Mussa A, Kalish JM.
europepmc   +1 more source

Beckwith-Wiedemann syndrome. [PDF]

Journal of Medical Genetics, 1992
A M Norman, A P Read, D Donnai
openaire   +1 more source