Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_provenance.
• NP83679.RAwO430tpMBxuoq3220Sxj5VFNvijSM-Zupff3JlG7B8Y130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83679.RAwO430tpMBxuoq3220Sxj5VFNvijSM-Zupff3JlG7B8Y130_provenance.
• NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_provenance.
• NP88190.RA6YIncj34hStrZBzqGQzugo9FQQYxwURvZdmPc__Bmrk130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88190.RA6YIncj34hStrZBzqGQzugo9FQQYxwURvZdmPc__Bmrk130_provenance.
• NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87581.RAc4q_sRJUJwJ3LeHvCMk0_oSCxEkF6zvkUvOU1qrN5-8130_provenance.
• NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92783.RA4MGzIgyCOmWidEMlQYoGLqUVy9xEPxXGcK4kXSRMIWA130_provenance.
• NP92671.RAudApDjuWFhAZ_KGM2-45KR4qPzv-LMcIxzkaIrAYFrQ130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92671.RAudApDjuWFhAZ_KGM2-45KR4qPzv-LMcIxzkaIrAYFrQ130_provenance.
• NP93067.RAuuSrPTLdGpIior--4hxh4ejl1vRppT_x5EHe5zJTi34130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93067.RAuuSrPTLdGpIior--4hxh4ejl1vRppT_x5EHe5zJTi34130_provenance.
• NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_provenance.
• NP129113.RAm8KaOZig0F2z7uS-hjWo-YyL1WsQS4G_zQV8vyYeRnA130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129113.RAm8KaOZig0F2z7uS-hjWo-YyL1WsQS4G_zQV8vyYeRnA130_provenance.
• NP150665.RApyv1KUCyYECSqY6h1cZHKO5DgBJIqaasKZ6OGKowo00130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150665.RApyv1KUCyYECSqY6h1cZHKO5DgBJIqaasKZ6OGKowo00130_provenance.
• NP151046.RAuub7wacm9dQ6YbB87J-Qb-eO2VCfdtp8umO1AQbie74130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151046.RAuub7wacm9dQ6YbB87J-Qb-eO2VCfdtp8umO1AQbie74130_provenance.
• NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151867.RAnGbb_ZgslRY_bUc33_xVVLL3UJHrlL4QREW81-iZRl0130_provenance.
• NP152068.RAAe67yVBR1EAuubKC2vhKuyIm4RrvKWqvnpycw7SNHFc130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152068.RAAe67yVBR1EAuubKC2vhKuyIm4RrvKWqvnpycw7SNHFc130_provenance.
• NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139573.RA6Jb3SZ_GAXhrmoVE9A4jmfyFi_fQ5dp-rwvRi-MtzfY130_provenance.
• NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_provenance.
• NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136798.RA__hQFRLlSJKCZDoFt6-MsDrLqiDtrFsSyz_vMcSSXjY130_provenance.
• NP141092.RAE0B8-oLrBqwAE9IxigNdZzpzowVs8EzwkdBT08ligFg130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141092.RAE0B8-oLrBqwAE9IxigNdZzpzowVs8EzwkdBT08ligFg130_provenance.