<--- Back to Details
First PageDocument Content
Genodermatoses / Syndromes / Small nuclear RNA / Epigenetics / Prader–Willi syndrome / Chromosomes / Genomic imprinting / Small nucleolar RNA SNORD116 / Angelman syndrome / Genetics / Biology / Health
Date: 2012-04-04 15:27:52
Genodermatoses
Syndromes
Small nuclear RNA
Epigenetics
Prader–Willi syndrome
Chromosomes
Genomic imprinting
Small nucleolar RNA SNORD116
Angelman syndrome
Genetics
Biology
Health

genetest review ©American College of Medical Genetics Prader-Willi syndrome Suzanne B. Cassidy, MD1, Stuart Schwartz, PhD2, Jennifer L. Miller, MD3 and Daniel J. Driscoll, MD, PhD4

Add to Reading List

Source URL: www.nature.com

Download Document from Source Website

File Size: 892,30 KB

Share Document on Facebook

Similar Documents

Prader-Willi Syndrome (PWS) First description Prader-Willi syndrome (PWS) was first described in 1956 by Prader, Labhart and Willi. Genetics and molecular biology PWS results from the absence of expression of the paterna

Prader-Willi Syndrome (PWS) First description Prader-Willi syndrome (PWS) was first described in 1956 by Prader, Labhart and Willi. Genetics and molecular biology PWS results from the absence of expression of the paterna

DocID: 19j07 - View Document

SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Prader-Willi Syndrome (PWS)

SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Prader-Willi Syndrome (PWS)

DocID: 14Mho - View Document

Discovery of new type of RNA could have implications for some congenital disorders

Discovery of new type of RNA could have implications for some congenital disorders

DocID: QsT8 - View Document

genetest review  ©American College of Medical Genetics Prader-Willi syndrome Suzanne B. Cassidy, MD1, Stuart Schwartz, PhD2, Jennifer L. Miller, MD3 and Daniel J. Driscoll, MD, PhD4

genetest review ©American College of Medical Genetics Prader-Willi syndrome Suzanne B. Cassidy, MD1, Stuart Schwartz, PhD2, Jennifer L. Miller, MD3 and Daniel J. Driscoll, MD, PhD4

DocID: uvd8 - View Document