Results
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26161.
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26162.
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26163.
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26164.
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26165.
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26166.
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26167.
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26168.
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Fine mapping of a region on chromosome 8p gives evidence for a QTL contributing to individual differences in an anxiety-related personality trait: TPQ harm avoidance. [electronic resource] by
- Dina, Christian
- Nemanov, Lubov
- Gritsenko, Inga
- Rosolio, Naama
- Osher, Yamima
- Heresco-Levy, Uri
- Sariashvilli, Emma
- Bachner-Melman, Rachel
- Zohar, Ada H
- Benjamin, Jonathan
- Belmaker, Robert H
- Ebstein, Richard P
Producer: 20050512
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 132B
Availability: No items available.
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26169.
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A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3. [electronic resource] by
- Kurz, T
- Altmueller, J
- Strauch, K
- Rüschendorf, F
- Heinzmann, A
- Moffatt, M F
- Cookson, W O C M
- Inacio, F
- Nürnberg, P
- Stassen, H H
- Deichmann, K A
Producer: 20050511
In:
Allergy vol. 60
Availability: No items available.
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26170.
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26171.
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26172.
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26173.
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A region on human chromosome 4 (q35.1-->qter) induces senescence in cell hybrids and is involved in cervical carcinogenesis. [electronic resource] by
- Backsch, Claudia
- Rudolph, Bettina
- Kühne-Heid, Rosemarie
- Kalscheuer, Vera
- Bartsch, Oliver
- Jansen, Lars
- Beer, Katrin
- Meyer, Birgit
- Schneider, Achim
- Dürst, Matthias
Producer: 20050726
In:
Genes, chromosomes & cancer vol. 43
Availability: No items available.
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26174.
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26175.
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26176.
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26177.
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26178.
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Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations. [electronic resource] by
- Charfeddine, C
- Monastiri, K
- Mokni, M
- Laadjimi, A
- Kaabachi, N
- Perin, O
- Nilges, M
- Kassar, S
- Keirallah, M
- Guediche, M N
- Kamoun, M R
- Tebib, N
- Ben Dridi, M F
- Boubaker, S
- Ben Osman, A
- Abdelhak, S
Producer: 20060627
In:
Molecular genetics and metabolism vol. 88
Availability: No items available.
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26179.
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26180.
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Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among northern Europeans. [electronic resource] by
- Gilling, Mette
- Dullinger, Jörn S
- Gesk, Stefan
- Metzke-Heidemann, Simone
- Siebert, Reiner
- Meyer, Thomas
- Brondum-Nielsen, Karen
- Tommerup, Niels
- Ropers, Hans-Hilger
- Tümer, Zeynep
- Kalscheuer, Vera M
- Thomas, N Simon
Producer: 20060609
In:
American journal of human genetics vol. 78
Availability: No items available.
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