A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome - Concepedia

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A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome

DOI Full Paper Access

134

Citations

30

References

2008

Year

Deniz Kanber, Jacques C. Giltay, Dagmar Wieczorek, Corinna Zogel, Ron Hochstenbach, Almuth Caliebe, Alma Kuechler, Bernhard Horsthemke, Karin Buiting

European Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsClinical GeneticsGenetic EpidemiologyPathologyNeurogeneticsMolecular GeneticsPaternal DeletionDisease Gene IdentificationPrader–willi SyndromeMedical GeneticsPublic HealthMedicineEpigeneticsDisorders Of Sex DevelopmentMonogenic Disorders

References

	Year	Citations

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