Matches in DBpedia 2016-04 for { <http://doi.org/10.1136/jmg.35.8.617> ?p ?o }
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- jmg.35.8.617 doi "10.1136/jmg.35.8.617".
- jmg.35.8.617 first1 "DR".
- jmg.35.8.617 first2 "GD".
- jmg.35.8.617 first3 "DT".
- jmg.35.8.617 first4 "BA".
- jmg.35.8.617 first5 "J".
- jmg.35.8.617 first6 "LC".
- jmg.35.8.617 first7 "NL".
- jmg.35.8.617 first8 "MJ".
- jmg.35.8.617 isCitedBy Mowat–Wilson_syndrome.
- jmg.35.8.617 issue "8".
- jmg.35.8.617 journal "Journal of Medical Genetics".
- jmg.35.8.617 last1 "Mowat".
- jmg.35.8.617 last2 "Croaker".
- jmg.35.8.617 last3 "Cass".
- jmg.35.8.617 last4 "Kerr".
- jmg.35.8.617 last5 "Chaitow".
- jmg.35.8.617 last6 "Adès".
- jmg.35.8.617 last7 "Chia".
- jmg.35.8.617 last8 "Wilson".
- jmg.35.8.617 pages "617–23".
- jmg.35.8.617 pmc "1051383".
- jmg.35.8.617 pmid "9719364".
- jmg.35.8.617 title "Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: Delineation of a new syndrome and identification of a locus at chromosome 2q22-q23".
- jmg.35.8.617 volume "35".
- jmg.35.8.617 year "1998".