Results
|
29281.
|
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11. [electronic resource] by
- Richter, A
- Rioux, J D
- Bouchard, J P
- Mercier, J
- Mathieu, J
- Ge, B
- Poirier, J
- Julien, D
- Gyapay, G
- Weissenbach, J
- Hudson, T J
- Melançon, S B
- Morgan, K
Producer: 19990420
In:
American journal of human genetics vol. 64
Availability: No items available.
|
|
29282.
|
|
|
29283.
|
Fractional allele loss indicates distinct genetic populations in the development of squamous cell carcinoma of the head and neck (SCCHN). [electronic resource] by
- Nunn, J
- Scholes, A G
- Liloglou, T
- Nagini, S
- Jones, A S
- Vaughan, E D
- Gosney, J R
- Rogers, S
- Fear, S
- Field, J K
Producer: 20000211
In:
Carcinogenesis vol. 20
Availability: No items available.
|
|
29284.
|
|
|
29285.
|
Structural analysis and evaluation of the 11beta-hydroxysteroid dehydrogenase type 2 (11beta-HSD2) gene in human essential hypertension. [electronic resource] by
- Brand, E
- Kato, N
- Chatelain, N
- Krozowski, Z S
- Jeunemaitre, X
- Corvol, P
- Plouin, P F
- Cambien, F
- Pascoe, L
- Soubrier, F
Producer: 19990305
In:
Journal of hypertension vol. 16
Availability: No items available.
|
|
29286.
|
|
|
29287.
|
|
|
29288.
|
|
|
29289.
|
|
|
29290.
|
|
|
29291.
|
|
|
29292.
|
|
|
29293.
|
|
|
29294.
|
|
|
29295.
|
|
|
29296.
|
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency. [electronic resource] by
- Lu, Yao Bang
- Kobayashi, Keiko
- Ushikai, Miharu
- Tabata, Ayako
- Iijima, Mikio
- Li, Meng Xian
- Lei, Lei
- Kawabe, Kotaro
- Taura, Satoru
- Yang, Yanling
- Liu, Tze-Tze
- Chiang, Szu-Hui
- Hsiao, Kwang-Jen
- Lau, Yu-Lung
- Tsui, Lap-Chee
- Lee, Dong Hwan
- Saheki, Takeyori
Producer: 20060105
In:
Journal of human genetics vol. 50
Availability: No items available.
|
|
29297.
|
|
|
29298.
|
|
|
29299.
|
Patients of African ancestry with hemophagocytic lymphohistiocytosis share a common haplotype of PRF1 with a 50delT mutation. [electronic resource] by
- Lee, Susan Molleran
- Sumegi, Janos
- Villanueva, Joyce
- Tabata, Yasuhiro
- Zhang, Kejian
- Chakraborty, Ranajit
- Sheng, Xiaohua
- Clementi, Rita
- de Saint Basile, Genevieve
- Filipovich, Alexandra H
Producer: 20060831
In:
The Journal of pediatrics vol. 149
Availability: No items available.
|
|
29300.
|
|