# Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1)

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/paediatric-phenotype-of-kallmann-syndrome-due-to-mutations-of-fibroblast-growth/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Delphine Zénaty,Patricia Bretones,Cécile Lambe,Isabelle Guemas,M David,Juliane Léger,Nicolás de Roux |
| Citations | 55 |
| DOI | 10.1016/j.mce.2006.04.006 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2155632713 |
| PMID | 16757108 |
| Type | article |
| Year | 2006 |

## Paper authors

- [Cécile Lambe](https://scholariq.org/researchers/cecile-lambe/)

## Paper primary topic

- [Fibroblast Growth Factor Research](https://scholariq.org/topics/fibroblast-growth-factor-research/)

## Paper topics

- [Fibroblast Growth Factor Research](https://scholariq.org/topics/fibroblast-growth-factor-research/)
- [Neonatal Respiratory Health Research](https://scholariq.org/topics/neonatal-respiratory-health-research/)
- [Neuroscience of respiration and sleep](https://scholariq.org/topics/neuroscience-of-respiration-and-sleep/)

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