Results
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Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia. [electronic resource] by
- Tekin, Mustafa
- Hişmi, Burcu Oztürk
- Fitoz, Suat
- Ozdağ, Hilal
- Cengiz, Filiz Başak
- Sirmaci, Asli
- Aslan, Idil
- Inceoğlu, Bora
- Yüksel-Konuk, E Berrin
- Yilmaz, Seda Taşir
- Yasun, Oztan
- Akar, Nejat
Producer: 20070313
In:
American journal of human genetics vol. 80
Availability: No items available.
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Comparison of clinical-radiological and molecular findings in hypochondroplasia. [electronic resource] by
- Prinster, C
- Carrera, P
- Del Maschio, M
- Weber, G
- Maghnie, M
- Vigone, M C
- Mora, S
- Tonini, G
- Rigon, F
- Beluffi, G
- Severi, F
- Chiumello, G
- Ferrari, M
Producer: 19980227
In:
American journal of medical genetics vol. 75
Availability: No items available.
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78.
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Hypomethylated Fgf3 is a potential biomarker for early detection of oral cancer in mice treated with the tobacco carcinogen dibenzo[def,p]chrysene. [electronic resource] by
- Sun, Yuan-Wan
- Chen, Kun-Ming
- Imamura Kawasawa, Yuka
- Salzberg, Anna C
- Cooper, Timothy K
- Caruso, Carla
- Aliaga, Cesar
- Zhu, Junjia
- Gowda, Krishne
- Amin, Shantu
- El-Bayoumy, Karam
Producer: 20171211
In:
PloS one vol. 12
Availability: No items available.
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80.
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Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further Cases. [electronic resource] by
- Al Yassin, Amina
- D'Arco, Felice
- Morín, Matías
- Pagarkar, Waheeda
- Harrop-Griffiths, Katherine
- Shaida, Azhar
- Fernández, Elena
- Cullup, Tom
- De-Souza, Bianca
- Moreno-Pelayo, Miguel Angel
- Bitner-Glindzicz, Maria
Producer: 20200102
In:
Genes vol. 10
Availability: No items available.
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