Matches in Nanopublications for { ?s ?p "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP365656.RA1RETWk10A1insXb5eTqSmU2fYdG3P4FF9awEpijAlIk130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365656.RA1RETWk10A1insXb5eTqSmU2fYdG3P4FF9awEpijAlIk130_provenance.
- NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556534.RApMYFytEKp-NaTLllFxWARrGc-hGAkG1uFs5ShAQt-sY130_provenance.
- NP850779.RAxuoZmNnoaAKODT8FEaA-LNHL238lNR_KwTHPq6ej4bg130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850779.RAxuoZmNnoaAKODT8FEaA-LNHL238lNR_KwTHPq6ej4bg130_provenance.
- assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP986749.RAi7fIKmASok21yAafTT3v-w2mHNIfVK2PcIdrMU7vGyc130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986749.RAi7fIKmASok21yAafTT3v-w2mHNIfVK2PcIdrMU7vGyc130_provenance.
- NP696097.RAMGnN2mF1eFyME688QkaiDDBPVP8mYrpoLMMA2jsyjdU130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696097.RAMGnN2mF1eFyME688QkaiDDBPVP8mYrpoLMMA2jsyjdU130_provenance.
- NP696105.RA_ATZK6YkBL-R2_R6n3umiREJ0G5ySr5XgxPshyTKGXU130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696105.RA_ATZK6YkBL-R2_R6n3umiREJ0G5ySr5XgxPshyTKGXU130_provenance.
- NP986746.RAw8n3H2yrbB84MP_m9WoklHuH1Bfq4Ys2gUXAybCN8Rg130_assertion description "[We studied SLC2A2 in patients with transient neonatal diabetes mellitus (TNDM; n = 25) or permanent neonatal diabetes mellitus (PNDM; n = 79) in whom we had excluded the common genetic causes of neonatal diabetes, using a combined approach of sequencing and homozygosity mapping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986746.RAw8n3H2yrbB84MP_m9WoklHuH1Bfq4Ys2gUXAybCN8Rg130_provenance.