Log in to save to my catalogue

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical t...

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical t...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_874181504

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins

About this item

Full title

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins

Publisher

Berlin/Heidelberg: Springer-Verlag

Journal title

European journal of pediatrics, 2010-02, Vol.169 (2), p.207-213

Language

English

Formats

Publication information

Publisher

Berlin/Heidelberg: Springer-Verlag

More information

Scope and Contents

Contents

One known genetic mechanism for transient neonatal diabetes is loss of methylation at 6q24. The etiology of prune belly sequence is unknown but a genetic defect, affecting the mesoderm from which the triad abdominal muscle hypoplasia, urinary tract abnormalities, and cryptorchidism develop, has been suggested. We investigated a family, including on...

Alternative Titles

Full title

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_874181504

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_874181504

Other Identifiers

ISSN

0340-6199

E-ISSN

1432-1076

DOI

10.1007/s00431-009-1008-y

How to access this item