Results
|
4321.
|
|
|
4322.
|
|
|
4323.
|
|
|
4324.
|
|
|
4325.
|
|
|
4326.
|
|
|
4327.
|
|
|
4328.
|
|
|
4329.
|
|
|
4330.
|
|
|
4331.
|
Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome. [electronic resource] by
- Stoetzel, Corinne
- Muller, Jean
- Laurier, Virginie
- Davis, Erica E
- Zaghloul, Norann A
- Vicaire, Serge
- Jacquelin, Cecile
- Plewniak, Frederic
- Leitch, Carmen C
- Sarda, Pierre
- Hamel, Christian
- de Ravel, Thomy J L
- Lewis, Richard Alan
- Friederich, Evelyne
- Thibault, Christelle
- Danse, Jean-Marc
- Verloes, Alain
- Bonneau, Dominique
- Katsanis, Nicholas
- Poch, Olivier
- Mandel, Jean-Louis
- Dollfus, Helene
Producer: 20070212
In:
American journal of human genetics vol. 80
Availability: No items available.
|
|
4332.
|
A mitochondrial stratigraphy for island southeast Asia. [electronic resource] by
- Hill, Catherine
- Soares, Pedro
- Mormina, Maru
- Macaulay, Vincent
- Clarke, Dougie
- Blumbach, Petya B
- Vizuete-Forster, Matthieu
- Forster, Peter
- Bulbeck, David
- Oppenheimer, Stephen
- Richards, Martin
Producer: 20070212
In:
American journal of human genetics vol. 80
Availability: No items available.
|
|
4333.
|
|
|
4334.
|
|
|
4335.
|
Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. [electronic resource] by
- Pearson, John V
- Huentelman, Matthew J
- Halperin, Rebecca F
- Tembe, Waibhav D
- Melquist, Stacey
- Homer, Nils
- Brun, Marcel
- Szelinger, Szabolcs
- Coon, Keith D
- Zismann, Victoria L
- Webster, Jennifer A
- Beach, Thomas
- Sando, Sigrid B
- Aasly, Jan O
- Heun, Reinhard
- Jessen, Frank
- Kolsch, Heike
- Tsolaki, Magdalini
- Daniilidou, Makrina
- Reiman, Eric M
- Papassotiropoulos, Andreas
- Hutton, Michael L
- Stephan, Dietrich A
- Craig, David W
Producer: 20070212
In:
American journal of human genetics vol. 80
Availability: No items available.
|
|
4336.
|
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation. [electronic resource] by
- Upadhyaya, M
- Huson, S M
- Davies, M
- Thomas, N
- Chuzhanova, N
- Giovannini, S
- Evans, D G
- Howard, E
- Kerr, B
- Griffiths, S
- Consoli, C
- Side, L
- Adams, D
- Pierpont, M
- Hachen, R
- Barnicoat, A
- Li, H
- Wallace, P
- Van Biervliet, J P
- Stevenson, D
- Viskochil, D
- Baralle, D
- Haan, E
- Riccardi, V
- Turnpenny, P
- Lazaro, C
- Messiaen, L
Producer: 20070212
In:
American journal of human genetics vol. 80
Availability: No items available.
|
|
4337.
|
|
|
4338.
|
|
|
4339.
|
|
|
4340.
|
|