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*  Beckwith-Wiedemann syndrome | Genetic and Rare Diseases Information Center (GARD) - an NCATS Program
Most cases of BWS are due to abnormalities involving genes on chromosome 11 that undergo genomic imprinting (imprinted genes).[ ... are due to a phenomenon called genomic imprinting. ... for imprinting when egg and sperm cells. are formed. BWS is ... often associated with changes in regions of DNA on chromosome 11 called imprinting centers (ICs), which control the methylation ...
https://rarediseases.info.nih.gov/diseases/3343/index
*  Pseudohypoparathyroidism type 1B | Genetic and Rare Diseases Information Center (GARD) - an NCATS Program
is inherited affects the way a gene acts, it is called genomic imprinting. PHP1B may be caused by randomly inheriting both ... This phenomenon is known as genomic imprinting.. In familial. cases of PHP1B, it appears that parathyroid hormone. (PTH) ...
https://rarediseases.info.nih.gov/diseases/10680/pseudohypoparathyroidism-type-1b