Results
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28001.
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Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28. [electronic resource] by
- Villard, L
- des Portes, V
- Levy, N
- Louboutin, J P
- Recan, D
- Coquet, M
- Chabrol, B
- Figarella-Branger, D
- Chelly, J
- Pellissier, J F
- Fontes, M
Producer: 20000512
In:
European journal of human genetics : EJHG vol. 8
Availability: No items available.
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28002.
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Localization of multiple melanoma tumor-suppressor genes on chromosome 11 by use of homozygosity mapping-of-deletions analysis. [electronic resource] by
- Goldberg, E K
- Glendening, J M
- Karanjawala, Z
- Sridhar, A
- Walker, G J
- Hayward, N K
- Rice, A J
- Kurera, D
- Tebha, Y
- Fountain, J W
Producer: 20000821
In:
American journal of human genetics vol. 67
Availability: No items available.
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28003.
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28004.
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28005.
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Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia. [electronic resource] by
- Lund, A
- Udd, B
- Juvonen, V
- Andersen, P M
- Cederquist, K
- Ronnevi, L O
- Sistonen, P
- Sörensen, S A
- Tranebjaerg, L
- Wallgren-Pettersson, C
- Savontaus, M L
Producer: 20001207
In:
European journal of human genetics : EJHG vol. 8
Availability: No items available.
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28006.
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28007.
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Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in Brazil. [electronic resource] by
- Raskin, S
- Phillips, J A
- Kaplan, G
- McClure, M
- Vnencak-Jones, C
- Rozov, T
- Cardieri, J M
- Marostica, P
- Abreu, F
- Giugliani, R
- Reis, F
- Rosario, N A
- Ludwig, N
- Pereira, L
- Faucz, F
- Gabardo, J
- Culpi, L
Producer: 19990305
In:
Human biology vol. 71
Availability: No items available.
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28008.
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Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. [electronic resource] by
- Ophoff, R A
- DeYoung, J
- Service, S K
- Joosse, M
- Caffo, N A
- Sandkuijl, L A
- Terwindt, G M
- Haan, J
- van den Maagdenberg, A M
- Jen, J
- Baloh, R W
- Barilla-LaBarca, M L
- Saccone, N L
- Atkinson, J P
- Ferrari, M D
- Freimer, N B
- Frants, R R
Producer: 20010816
In:
American journal of human genetics vol. 69
Availability: No items available.
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28009.
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28010.
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28011.
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28012.
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A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder. [electronic resource] by
- DeLisi, Lynn E
- Shaw, Sarah H
- Crow, Timothy J
- Shields, Gail
- Smith, Angela B
- Larach, Veronica W
- Wellman, Nigel
- Loftus, Josephine
- Nanthakumar, Betsy
- Razi, Kamran
- Stewart, John
- Comazzi, Margherita
- Vita, Antonio
- Heffner, Thomas
- Sherrington, Robin
Producer: 20020603
In:
The American journal of psychiatry vol. 159
Availability: No items available.
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28013.
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Frameshift mutations of human gastrin receptor gene (hGARE) in gastrointestinal cancers with microsatellite instability. [electronic resource] by
- Laghi, Luigi
- Ranzani, Guglielmina Nadia
- Bianchi, Paolo
- Mori, Antonio
- Heinimann, Karl
- Orbetegli, Ombretta
- Spaudo, Marco Rondo
- Luinetti, Ombretta
- Francisconi, Simona
- Roncalli, Massimo
- Solcia, Enrico
- Malesci, Alberto
Producer: 20020404
In:
Laboratory investigation; a journal of technical methods and pathology vol. 82
Availability: No items available.
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28014.
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28015.
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28016.
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28017.
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28018.
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28019.
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28020.
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