ScholarLens Back to search
2016•The Japanese Society for Pediatric EndocrinologyRequires access

10p deletion in DiGeorge Syndrome Phenotype and Hypoparathyroidism: A case report

Ediz Yeşilkaya

Open publisher page 0 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Hypoparathyroidism, DiGeorge syndrome, Phenotype, Internal medicine, Medicine, Endocrinology, Biology, Genetics

Back to paper searchBrowse research topicsOriginal source
10p deletion in DiGeorge Syndrome Phenotype and Hypoparathyroidism: A case report — Research Paper | ScholarLens