Results
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32941.
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32942.
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32943.
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32944.
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Isolated loss of PMS2 expression in colorectal cancers: frequency, patient age, and familial aggregation. [electronic resource] by
- Gill, Sharlene
- Lindor, Noralane M
- Burgart, Lawrence J
- Smalley, Regenia
- Leontovich, Olga
- French, Amy J
- Goldberg, Richard M
- Sargent, Daniel J
- Jass, Jeremy R
- Hopper, John L
- Jenkins, Mark A
- Young, Joanne
- Barker, Melissa A
- Walsh, Michael D
- Ruszkiewicz, Andrew R
- Thibodeau, Stephen N
Producer: 20051108
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 11
Availability: No items available.
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32945.
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Characterization of familial non-BRCA1/2 breast tumors by loss of heterozygosity and immunophenotyping. [electronic resource] by
- Oldenburg, Rogier A
- Kroeze-Jansema, Karin
- Meijers-Heijboer, Hanne
- van Asperen, Cristi J
- Hoogerbrugge, Nicoline
- van Leeuwen, Inge
- Vasen, Hans F A
- Cleton-Jansen, Anne-Marie
- Kraan, Jaennelle
- Houwing-Duistermaat, Jeanine J
- Morreau, Hans
- Cornelisse, Cees J
- Devilee, Peter
Producer: 20061127
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 12
Availability: No items available.
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32946.
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32947.
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TEL deletion analysis supports a novel view of relapse in childhood acute lymphoblastic leukemia. [electronic resource] by
- Zuna, Jan
- Ford, Anthony M
- Peham, Martina
- Patel, Naina
- Saha, Vaskar
- Eckert, Cornelia
- Köchling, Joachim
- Panzer-Grümayer, Renate
- Trka, Jan
- Greaves, Mel
Producer: 20050217
In:
Clinical cancer research : an official journal of the American Association for Cancer Research vol. 10
Availability: No items available.
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32948.
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32949.
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A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardation. [electronic resource] by
- Genevieve, D
- Baumann, C
- Huber, C
- Faivre, L
- Sanlaville, D
- Bodemer, C
- Hadj-Rabia, S
- Assoumou, A
- Verloes, A
- Raqbi, F
- Munnich, A
- Cormier-Daire, V
Producer: 20040927
In:
Journal of medical genetics vol. 41
Availability: No items available.
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32950.
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32951.
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32952.
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32953.
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32954.
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32955.
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32956.
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32957.
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32958.
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Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations. [electronic resource] by
- Lines, Matthew A
- Kozlowski, Kathy
- Kulak, Stephen C
- Allingham, R Rand
- Héon, Elise
- Ritch, Robert
- Levin, Alex V
- Shields, M Bruce
- Damji, Karim F
- Newlin, Anna
- Walter, Michael A
Producer: 20040318
In:
Investigative ophthalmology & visual science vol. 45
Availability: No items available.
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32959.
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32960.
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