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Paediatric oncology
Citations 91-94 of 94 total displayed.
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Past content
(since Jan 1999):
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Original articles
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation
- Wayne W K Lam, Izuho Hatada, Sachiko Ohishi, Tsunehiro Mukai, Johanna A Joyce, Trevor R P Cole, Dian Donnai, Wolf Reik, Paul N Schofield, Eamonn R Maher
J. Med. Genet. 1999; 36: 518-523.
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Original articles
Association of a lymphotoxin gene polymorphism and atopy in Italian families
- Elisabetta Trabetti, Cristina Patuzzo, Giovanni Malerba, Roberta Galavotti, Laura Carmen Martinati, Attilio L Boner, Pier Franco Pignatti
J. Med. Genet. 1999; 36: 323-325.
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Short reports
A small interstitial deletion in the GPC3 gene causes Simpson-Golabi-Behmel syndrome in a Dutch-Canadian family
- Jian Y Xuan, Rhiannon M Hughes-Benzie, Alex E MacKenzie
J. Med. Genet. 1999; 36: 57-58.
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Short reports
Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3' APC mutation
- Alex Kartheuser, Corinne Walon, Sarah West, Cor Breukel, Roger Detry, Anne-Catherine Gribomont, Tayebeh Hamzehloei, Pierre Hoang, Dominique Maiter, Jacques Pringot, Jacques Rahier, P Meera Khan, Ann Curtis, John Burn, Riccardo Fodde, Christine Verellen-Dumoulin
J. Med. Genet. 1999; 36: 65-67.
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