Results
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DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics. [electronic resource] by
- Vona, B
- Hofrichter, M A H
- Neuner, C
- Schröder, J
- Gehrig, A
- Hennermann, J B
- Kraus, F
- Shehata-Dieler, W
- Klopocki, E
- Nanda, I
- Haaf, T
Producer: 20150820
In:
Clinical genetics vol. 87
Availability: No items available.
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The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. [electronic resource] by
- Dal Zotto, L
- Quaderi, N A
- Elliott, R
- Lingerfelter, P A
- Carrel, L
- Valsecchi, V
- Montini, E
- Yen, C H
- Chapman, V
- Kalcheva, I
- Arrigo, G
- Zuffardi, O
- Thomas, S
- Willard, H F
- Ballabio, A
- Disteche, C M
- Rugarli, E I
Producer: 19980416
In:
Human molecular genetics vol. 7
Availability: No items available.
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Expression of OCT4 pseudogenes in human tumours: lessons from glioma and breast carcinoma. [electronic resource] by
- Zhao, Shidou
- Yuan, Qiuhuan
- Hao, Hongbo
- Guo, Yuji
- Liu, Shangming
- Zhang, Yanmin
- Wang, Jianli
- Liu, Huijuan
- Wang, Fuwu
- Liu, Kai
- Ling, Eng-Ang
- Hao, Aijun
Producer: 20110602
In:
The Journal of pathology vol. 223
Availability: No items available.
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3300.
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Improved multiplex ligation-dependent probe amplification analysis identifies a deleterious PMS2 allele generated by recombination with crossover between PMS2 and PMS2CL. [electronic resource] by
- Wernstedt, Annekatrin
- Valtorta, Emanuele
- Armelao, Franco
- Togni, Roberto
- Girlando, Salvatore
- Baudis, Michael
- Heinimann, Karl
- Messiaen, Ludwine
- Staehli, Noemie
- Zschocke, Johannes
- Marra, Giancarlo
- Wimmer, Katharina
Producer: 20121129
In:
Genes, chromosomes & cancer vol. 51
Availability: No items available.
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