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27541.
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27542.
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27543.
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Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population. [electronic resource] by
- Hildebrand, Michael S
- Kahrizi, Kimia
- Bromhead, Catherine J
- Shearer, A Eliot
- Webster, Jennifer A
- Khodaei, Hossein
- Abtahi, Rezvan
- Bazazzadegan, Niloofar
- Babanejad, Mojgan
- Nikzat, Nooshin
- Kimberling, William J
- Stephan, Dietrich
- Huygen, Patrick L M
- Bahlo, Melanie
- Smith, Richard J H
- Najmabadi, Hossein
Producer: 20110223
In:
The Annals of otology, rhinology, and laryngology vol. 119
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27544.
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27545.
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27546.
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Transcriptome sequencing and analysis of wild Amur Ide (Leuciscus waleckii) inhabiting an extreme alkaline-saline lake reveals insights into stress adaptation. [electronic resource] by
- Xu, Jian
- Ji, Peifeng
- Wang, Baosen
- Zhao, Lan
- Wang, Jian
- Zhao, Zixia
- Zhang, Yan
- Li, Jiongtang
- Xu, Peng
- Sun, Xiaowen
Producer: 20131022
In:
PloS one vol. 8
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27547.
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27548.
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Sweet drinks are made of this: conservation genetics of an endemic palm species from the Dominican Republic. [electronic resource] by
- Namoff, Sandra
- Veloz, Alberto
- Jiménez, Francisco
- Rodríguez-Peña, Rosa A
- Peguero, Brígido
- Lewis, Carl
- Moynihan, Jeremy
- Abdo, Melissa
- Maunder, Mike
- Von Wettberg, Eric
- Meerow, Alan W
- Griffith, M Patrick
- Francisco-Ortega, Javier
Producer: 20110421
In:
The Journal of heredity vol. 102
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27549.
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27550.
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27551.
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27552.
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27553.
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27554.
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27555.
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TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis. [electronic resource] by
- Cangul, Hakan
- Aycan, Zehra
- Saglam, Halil
- Forman, Julia R
- Cetinkaya, Semra
- Tarim, Omer
- Bober, Ece
- Cesur, Yasar
- Kurtoglu, Selim
- Darendeliler, Feyza
- Bas, Veysel
- Eren, Erdal
- Demir, Korcan
- Kiraz, Aslihan
- Aydin, Banu K
- Karthikeyan, Ambika
- Kendall, Michaela
- Boelaert, Kristien
- Shaw, Nick J
- Kirk, Jeremy
- Högler, Wolfgang
- Barrett, Timothy G
- Maher, Eamonn R
Producer: 20120904
In:
Journal of pediatric endocrinology & metabolism : JPEM vol. 25
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27556.
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Pentanucleotide repeat-primed PCR for genetic diagnosis of spinocerebellar ataxia type 31. [electronic resource] by
- Ishige, Takayuki
- Sawai, Setsu
- Itoga, Sakae
- Sato, Kenichi
- Utsuno, Emi
- Beppu, Minako
- Kanai, Kazuaki
- Nishimura, Motoi
- Matsushita, Kazuyuki
- Kuwabara, Satoshi
- Nomura, Fumio
Producer: 20131105
In:
Journal of human genetics vol. 57
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27557.
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27558.
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27559.
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27560.
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Hereditary breast cancer in Middle Eastern and North African (MENA) populations: identification of novel, recurrent and founder BRCA1 mutations in the Tunisian population. [electronic resource] by
- Mahfoudh, Wijden
- Bouaouina, Noureddine
- Ahmed, Slim Ben
- Gabbouj, Sallouha
- Shan, Jingxuan
- Mathew, Rebecca
- Uhrhammer, Nancy
- Bignon, Yves-Jean
- Troudi, Wafa
- Elgaaied, Amel Ben Ammar
- Hassen, Elham
- Chouchane, Lotfi
Producer: 20120501
In:
Molecular biology reports vol. 39
Availability: No items available.
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