Results
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4081.
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4082.
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4083.
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4084.
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4085.
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4086.
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4087.
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4088.
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4089.
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CTLA4 polymorphisms in minimal change nephrotic syndrome in children: a case-control study. [electronic resource] by
- Ohl, Kim
- Eberhardt, Christiane
- Spink, Clemens
- Zahn, Katharina
- Wagner, Norbert
- Eggermann, Thomas
- Kemper, Markus J
- Querfeld, Uwe
- Hoppe, Bernd
- Harendza, Sigrid
- Tenbrock, Klaus
Producer: 20140714
In:
American journal of kidney diseases : the official journal of the National Kidney Foundation vol. 63
Availability: No items available.
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4090.
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4091.
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4092.
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Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. [electronic resource] by
- Jinks, Robert N
- Puffenberger, Erik G
- Baple, Emma
- Harding, Brian
- Crino, Peter
- Fogo, Agnes B
- Wenger, Olivia
- Xin, Baozhong
- Koehler, Alanna E
- McGlincy, Madeleine H
- Provencher, Margaret M
- Smith, Jeffrey D
- Tran, Linh
- Al Turki, Saeed
- Chioza, Barry A
- Cross, Harold
- Harlalka, Gaurav V
- Hurles, Matthew E
- Maroofian, Reza
- Heaps, Adam D
- Morton, Mary C
- Stempak, Lisa
- Hildebrandt, Friedhelm
- Sadowski, Carolin E
- Zaritsky, Joshua
- Campellone, Kenneth
- Morton, D Holmes
- Wang, Heng
- Crosby, Andrew
- Strauss, Kevin A
Producer: 20151013
In:
Brain : a journal of neurology vol. 138
Availability: No items available.
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4093.
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4094.
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4095.
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4100.
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