A Novel Mutation Involving the Initiation Codon of FGF3 in a Family Described with Complete Inner Ear Agenesis, Microtia and Major Microdontia (LAMM Syndrome)
- DOI
- 10.4172/2157-7412.1000251
- Published
- 2014-10-31
- Container
- J Genet Syndr Gene Ther
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.4172/2157-7412.1000251,
title = {A Novel Mutation Involving the Initiation Codon of FGF3 in a Family Described with Complete Inner Ear Agenesis, Microtia and Major Microdontia (LAMM Syndrome)},
author = {Elise Schaefer and Maryline Minoux and Julia Lauer and Valérie Pelletier and Matthieu Schmittbuhl and Marie-Cécile Manière and François Clauss and Francis Veillon and Sophie Riehm and Corinne Stoetzel and Helene Dollfus},
year = {2014},
journal = {J Genet Syndr Gene Ther},
doi = {10.4172/2157-7412.1000251},
url = {https://doi.org/10.4172/2157-7412.1000251}
}RIS
TY - JOUR TI - A Novel Mutation Involving the Initiation Codon of FGF3 in a Family Described with Complete Inner Ear Agenesis, Microtia and Major Microdontia (LAMM Syndrome) AU - Elise Schaefer AU - Maryline Minoux AU - Julia Lauer AU - Valérie Pelletier AU - Matthieu Schmittbuhl AU - Marie-Cécile Manière AU - François Clauss AU - Francis Veillon AU - Sophie Riehm AU - Corinne Stoetzel AU - Helene Dollfus PY - 2014 JO - J Genet Syndr Gene Ther DO - 10.4172/2157-7412.1000251 UR - https://doi.org/10.4172/2157-7412.1000251 ER -
APA
Schaefer, E., Minoux, M., Lauer, J., Pelletier, V., Schmittbuhl, M., Manière, M., Clauss, F., Veillon, F., Riehm, S., Stoetzel, C., & Dollfus, H. (2014). A Novel Mutation Involving the Initiation Codon of FGF3 in a Family Described with Complete Inner Ear Agenesis, Microtia and Major Microdontia (LAMM Syndrome). J Genet Syndr Gene Ther. https://doi.org/10.4172/2157-7412.1000251
Source records
- hal · retrieved 2026-09-25T20:43:24.252Z