Paternal uniparental disomy 14 and related disorders

Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype

(2012) Masayo Kagami et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Prenatal findings of paternal uniparental disomy 14: Delineation of further patient

(2010) Nobuhiro Suzumori et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Prenatal findings of paternal uniparental disomy 14: Report of four patients

(2010) Michiko Yamanaka et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers

(2010) Masayo Kagami et al.   PLoS Genetics

Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2–H19 domain in bodies and placentas

(2008) Kazuki Yamazawa et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta

(2008) Yoichi Sekita et al.   NATURE GENETICS

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

(2008) Masayo Kagami et al.   NATURE GENETICS

Placentomegaly in Paternal Uniparental Disomy for Human Chromosome 14

(2008) M. Kagami et al.   PLACENTA

Genomic imprinting at the mammalian Dlk1-Dio3 domain

(2008) Simao Teixeira da Rocha et al.   TRENDS IN GENETICS