Methylation status of the KCNQ1OTand H19 genes in beckwith-wiedemann syndrome
Egyptian Journal of Medical Human Genetics [The]. 2005; 6 (1): 55-61
in En
| IMEMR
| ID: emr-70493
Responsible library:
EMRO
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Index:
IMEMR
Main subject:
Phenotype
/
Congenital Abnormalities
/
Chromosomes, Human, Pair 2
/
Blotting, Southern
/
Chromatography, High Pressure Liquid
/
DNA Methylation
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Egypt. J. Med. Hum. Genet.
Year:
2005