Results
|
|
1981.
|
|
|
|
1982.
|
|
|
|
1983.
|
|
|
|
1984.
|
|
|
|
1985.
|
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. [electronic resource] by
- Lorenz-Depiereux, Bettina
- Bastepe, Murat
- Benet-Pagès, Anna
- Amyere, Mustapha
- Wagenstaller, Janine
- Müller-Barth, Ursula
- Badenhoop, Klaus
- Kaiser, Stephanie M
- Rittmaster, Roger S
- Shlossberg, Alan H
- Olivares, José L
- Loris, César
- Ramos, Feliciano J
- Glorieux, Francis
- Vikkula, Miikka
- Jüppner, Harald
- Strom, Tim M
Producer: 20070118
In:
Nature genetics vol. 38
Availability: No items available.
|
|
|
1986.
|
|
|
|
1987.
|
|
|
|
1988.
|
|
|
|
1989.
|
|
|
|
1990.
|
|
|
|
1991.
|
|
|
|
1992.
|
|
|
|
1993.
|
|
|
|
1994.
|
|
|
|
1995.
|
|
|
|
1996.
|
|
|
|
1997.
|
Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. [electronic resource] by
- Konrad, Martin
- Schaller, Andre
- Seelow, Dominik
- Pandey, Amit V
- Waldegger, Siegfried
- Lesslauer, Annegret
- Vitzthum, Helga
- Suzuki, Yoshiro
- Luk, John M
- Becker, Christian
- Schlingmann, Karl P
- Schmid, Marcel
- Rodriguez-Soriano, Juan
- Ariceta, Gema
- Cano, Francisco
- Enriquez, Ricardo
- Juppner, Harald
- Bakkaloglu, Sevcan A
- Hediger, Matthias A
- Gallati, Sabina
- Neuhauss, Stephan C F
- Nurnberg, Peter
- Weber, Stefanie
Producer: 20061204
In:
American journal of human genetics vol. 79
Availability: No items available.
|
|
|
1998.
|
|
|
|
1999.
|
|
|
|
2000.
|
|