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Matches in Nanopublications for { ?s ?p "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP184522.RAV9cDopa8AIF3yox2Mtf_rfCZiLGS-AaVpcNMOjMqvds130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184522.RAV9cDopa8AIF3yox2Mtf_rfCZiLGS-AaVpcNMOjMqvds130_provenance.
• NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465406.RA5eV2oadfJfntScYdMY8Bxr_PItc-PXWbyO21y6J-Vd0130_provenance.
• NP790551.RASB0fvSaz3OKCvvJWWmALB0dqYQer2qTLCaBFfZjHwsI130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790551.RASB0fvSaz3OKCvvJWWmALB0dqYQer2qTLCaBFfZjHwsI130_provenance.
• assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1393930.RASYm3JuxPz5vxEIXgUbxLc2Ye4ijO90n89mB9DWH5Ty8130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393930.RASYm3JuxPz5vxEIXgUbxLc2Ye4ijO90n89mB9DWH5Ty8130_provenance.
• NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
• NP748897.RAMpzBoJgZyStNQlu-emrFKTcjxdzuo78uT6vTdK0_llY130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748897.RAMpzBoJgZyStNQlu-emrFKTcjxdzuo78uT6vTdK0_llY130_provenance.
• NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393931.RAmBTuPhCSfHmc82Z1ED7SdzclTSpWHmR2YzscH_y-dXY130_provenance.
• NP667124.RAP47O0okJLVAtGAG8ieepX3Sfb_yN1estmzyKqhkQZGI130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667124.RAP47O0okJLVAtGAG8ieepX3Sfb_yN1estmzyKqhkQZGI130_provenance.