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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
Search on Google
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