Results
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3301.
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3302.
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3303.
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Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States. [electronic resource] by
- Kurzawski, G
- Suchy, J
- Kładny, J
- Safranow, K
- Jakubowska, A
- Elsakov, P
- Kucinskas, V
- Gardovski, J
- Irmejs, A
- Sibul, H
- Huzarski, T
- Byrski, T
- Debniak, T
- Cybulski, C
- Gronwald, J
- Oszurek, O
- Clark, J
- Góźdź, S
- Niepsuj, S
- Słomski, R
- Pławski, A
- Łacka-Wojciechowska, A
- Rozmiarek, A
- Fiszer-Maliszewska, Ł
- Bebenek, M
- Sorokin, D
- Stawicka, M
- Godlewski, D
- Richter, P
- Brozek, I
- Wysocka, B
- Jawień, A
- Banaszkiewicz, Z
- Kowalczyk, J
- Czudowska, D
- Goretzki, P E
- Moeslein, G
- Lubiński, J
Producer: 20021213
In:
Journal of medical genetics vol. 39
Availability: No items available.
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3304.
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Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay. [electronic resource] by
- Sarroca, C
- Alfano, N
- Bendin, G T
- Della Valle, A
- Dominguez, A
- Quadrelli, R
- Vaglio, A
- Mechoso, B
- Tinley, S T
- Harty, A E
- Lynch, J F
- Franklin, B A
- Kristo, P
- Smyrk, T C
- Peltomäki, P
- Lynch, H T
Producer: 20000331
In:
Diseases of the colon and rectum vol. 43
Availability: No items available.
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3305.
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3306.
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3307.
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3308.
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3309.
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3310.
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3311.
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Distinct patterns of germ-line deletions in MLH1 and MSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC). [electronic resource] by
- Li, Lili
- McVety, Susan
- Younan, Rami
- Liang, Ping
- Du Sart, Desirée
- Gordon, Philip H
- Hutter, Pierre
- Hogervorst, Frans B L
- Chong, George
- Foulkes, William D
Producer: 20061226
In:
Human mutation vol. 27
Availability: No items available.
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3312.
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3313.
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3314.
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Tumour-specific methylation of PTPRG intron 1 locus in sporadic and Lynch syndrome colorectal cancer. [electronic resource] by
- van Roon, Eddy H J
- de Miranda, Noël F C C
- van Nieuwenhuizen, Merlijn P
- de Meijer, Emile J
- van Puijenbroek, Marjo
- Yan, Pearlly S
- Huang, Tim H-M
- van Wezel, Tom
- Morreau, Hans
- Boer, Judith M
Producer: 20110531
In:
European journal of human genetics : EJHG vol. 19
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3315.
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3316.
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3317.
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Evaluation of the colorectal cancer risk conferred by rare UNC5C alleles. [electronic resource] by
- Küry, Sébastien
- Garrec, Céline
- Airaud, Fabrice
- Breheret, Flora
- Guibert, Virginie
- Frenard, Cécile
- Jiao, Shuo
- Bonneau, Dominique
- Berthet, Pascaline
- Bossard, Céline
- Ingster, Olivier
- Cauchin, Estelle
- Bezieau, Stéphane
Producer: 20140715
In:
World journal of gastroenterology vol. 20
Availability: No items available.
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3318.
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3319.
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New EPCAM founder deletion in Polish population. [electronic resource] by
- Dymerska, D
- Gołębiewska, K
- Kuświk, M
- Rudnicka, H
- Scott, R J
- Billings, R
- Pławski, A
- Boruń, P
- Siołek, M
- Kozak-Klonowska, B
- Szwiec, M
- Kilar, E
- Huzarski, T
- Byrski, T
- Lubiński, J
- Kurzawski, G
Producer: 20180703
In:
Clinical genetics vol. 92
Availability: No items available.
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3320.
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Lynch-like syndrome is as frequent as Lynch syndrome in early-onset nonfamilial nonpolyposis colorectal cancer. [electronic resource] by
- Antelo, Marina
- Golubicki, Mariano
- Roca, Enrique
- Mendez, Guillermo
- Carballido, Marcela
- Iseas, Soledad
- Cuatrecasas, Miriam
- Moreira, Leticia
- Sanchez, A
- Carballal, S
- Castells, Antoni
- Boland, Clement R
- Goel, Ajay
- Balaguer, Francesc
Producer: 20191210
In:
International journal of cancer vol. 145
Availability: No items available.
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