Results
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31341.
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31342.
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31343.
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31344.
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A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability. [electronic resource] by
- Caluseriu, O
- Di Gregorio, C
- Lucci-Cordisco, E
- Santarosa, M
- Trojan, J
- Brieger, A
- Benatti, P
- Pedroni, M
- Colibazzi, T
- Bellacosa, A
- Neri, G
- Ponz de Leon, M
- Viel, A
- Genuardi, M
Producer: 20040615
In:
Journal of medical genetics vol. 41
Availability: No items available.
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31345.
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31346.
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31347.
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31348.
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Mapping of a novel susceptibility locus suggests a role for MC3R and CTSZ in human tuberculosis. [electronic resource] by
- Cooke, Graham S
- Campbell, Sarah J
- Bennett, Steve
- Lienhardt, Christian
- McAdam, Keith P W J
- Sirugo, Giorgio
- Sow, Oumou
- Gustafson, Per
- Mwangulu, Frank
- van Helden, Paul
- Fine, Paul
- Hoal, Eileen G
- Hill, Adrian V S
Producer: 20080813
In:
American journal of respiratory and critical care medicine vol. 178
Availability: No items available.
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31349.
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Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice. [electronic resource] by
- Fogelgren, Ben
- Kuroyama, Mari C
- McBratney-Owen, Brandeis
- Spence, Allyson A
- Malahn, Laura E
- Anawati, Mireille K
- Cabatbat, Chantelle
- Alarcon, Vernadeth B
- Marikawa, Yusuke
- Lozanoff, Scott
Producer: 20081210
In:
Developmental dynamics : an official publication of the American Association of Anatomists vol. 237
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31350.
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31356.
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Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. [electronic resource] by
- Riazuddin, Saima
- Anwar, Saima
- Fischer, Martin
- Ahmed, Zubair M
- Khan, Shahid Y
- Janssen, Audrey G H
- Zafar, Ahmad U
- Scholl, Ute
- Husnain, Tayyab
- Belyantseva, Inna A
- Friedman, Penelope L
- Riazuddin, Sheikh
- Friedman, Thomas B
- Fahlke, Christoph
Producer: 20090923
In:
American journal of human genetics vol. 85
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31357.
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31358.
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31359.
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31360.
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A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family. [electronic resource] by
- Yang, Guoxing
- Xing, Baogang
- Liu, Guangcai
- Lu, Xiangqing
- Jia, Xingang
- Lu, Xiangqing
- Wang, Xiuli
- Yu, Hongyan
- Fu, Yanjiang
- Zhao, Jialiang
Producer: 20110908
In:
Molecular vision vol. 17
Availability: No items available.
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