Placentomegaly in Paternal Uniparental Disomy for Human Chromosome 14

Author:

Kagami M.,Yamazawa K.,Matsubara K.,Matsuo N.,Ogata T.

Publisher

Elsevier BV

Subject

Developmental Biology,Obstetrics and Gynaecology,Reproductive Medicine

Reference12 articles.

1. Segmental and full paternal isodisomy for chromosome 14 in three patients: narrowing the critical region and implication for the clinical features;Kagami;Am J Med Genet A,2005

2. Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes;Kagami;Nat Genet,2008

3. Imprinted genes, placental development and fetal growth;Fowden;Horm Res,2006

4. Placental hypoplasia in maternal uniparental disomy for chromosome 7;Yamazawa;Am J Med Genet A,2008

5. Yamazawa K, Kagami M, Nagai T, Kondoh T, Onigata K, Maeyama K, et al. 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. J Mol Med, in press.

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