ven pongal Tamil
Selected indexed studies
- Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. (Am J Hum Genet, 2020) [PMID:32891193]
- Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. (J Am Soc Nephrol, 2018) [PMID:30143558]
- On Leucoderm, Vitiligo, Ven Kuttam (Tamil) or Cabbare (Singhalese), and Several New Methods of Treatment. (Br Med J, 1885) [PMID:20751240]
_Worker-drafted node — pending editorial review._
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Sources
- Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. (2020) pubmed
- Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. (2018) pubmed
- On Leucoderm, Vitiligo, Ven Kuttam (Tamil) or Cabbare (Singhalese), and Several New Methods of Treatment. (1885) pubmed
- Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract. (2017) pubmed
- A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux. (2018) pubmed
- Accuracy of filter paper method for measuring glycated hemoglobin. (2007) pubmed