# Pseudohypoparathyroidism and<i>GNAS</i>Epigenetic Defects: Clinical Evaluation of Albright Hereditary Osteodystrophy and Molecular Analysis in 40 Patients

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/pseudohypoparathyroidism-and-i-gnas-i-epigenetic-defects-clinical-evaluation-of/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Giovanna Mantovani,Luisa De Sanctis,Anna Maria Barbieri,Francesca Marta Elli,Valentina Bollati,Valentina Vaira,Pamela Labarile,Sara Bondioni,Erika Peverelli,Andrea Lania,Paolo Beck-Peccoz,Anna Spada |
| Citations | 148 |
| DOI | 10.1210/jc.2009-0176 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | true |
| OA Status | green |
| OA URL | http://hdl.handle.net/2434/156610 |
| OpenAlex ID | https://openalex.org/W2080184121 |
| PMID | 20061437 |
| Type | article |
| Year | 2010 |

## Paper authors

- [Luisa De Sanctis](https://scholariq.org/researchers/luisa-de-sanctis/)

## Paper journal

- [The Journal of Clinical Endocrinology & Metabolism](https://scholariq.org/journals/the-journal-of-clinical-endocrinology-and-metabolism/)

## Paper primary topic

- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Paper topics

- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.