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PRKACA‐related, atrial defects‐polydactyly‐multiple congenital malformation syndrome in an Indian patient.
Published in:
American Journal of Medical Genetics. Part A, 2024, v. 194, n. 7, p. 1, doi. 10.1002/ajmg.a.63566
By:
- Sithambaram, Sivagamy;
- Jacob, Prince;
- Neethukrishna, Kausthubham;
- Bhavani, Gandham SriLakshmi;
- Dalal, Ashwin;
- Shah, Hitesh;
- Girisha, Katta Mohan
Publication type:
Article
Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.
Published in:
2021
By:
- Levy, Michael A.;
- Beck, David B.;
- Metcalfe, Kay;
- Douzgou, Sofia;
- Sithambaram, Sivagamy;
- Cottrell, Trudie;
- Ansar, Muhammad;
- Kerkhof, Jennifer;
- Mignot, Cyril;
- Nougues, Marie-Christine;
- Keren, Boris;
- Moore, Hannah W.;
- Oegema, Renske;
- Giltay, Jacques C.;
- Simon, Marleen;
- van Jaarsveld, Richard H.;
- Bos, Jessica;
- van Haelst, Mieke;
- Motazacker, M. Mahdi;
- Boon, Elles M. J.
Publication type:
Correction Notice
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.
Published in:
NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00256-y
By:
- Levy, Michael A.;
- Beck, David B.;
- Metcalfe, Kay;
- Douzgou, Sofia;
- Sithambaram, Sivagamy;
- Cottrell, Trudie;
- Ansar, Muhammad;
- Kerkhof, Jennifer;
- Mignot, Cyril;
- Nougues, Marie-Christine;
- Keren, Boris;
- Moore, Hannah W.;
- Oegema, Renske;
- Giltay, Jacques C.;
- Simon, Marleen;
- van Jaarsveld, Richard H.;
- Bos, Jessica;
- van Haelst, Mieke;
- Motazacker, M. Mahdi;
- Boon, Elles M. J.
Publication type:
Article
A 7-year-old boy with dysphagia and proximal muscle weakness.
Published in:
2017
By:
- Sithambaram, Sivagamy;
- Tripathi, Neeta;
- Gopal-Kothandapani, Jaya Sujatha;
- Mordekar, Santosh
Publication type:
Case Study

Found: 4

PRKACA‐related, atrial defects‐polydactyly‐multiple congenital malformation syndrome in an Indian patient.

Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.

Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.

A 7-year-old boy with dysphagia and proximal muscle weakness.