A germline deletion of p14 ARF but not CDKN2A in a melanoma–neural system tumour syndrome family

By Newton Bishop J.  

Human Molecular Genetics, Vol. 10, Iss. 1, 2001-01 ,pp. : 55-62

Oxford University Press

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Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma

By Ghiorzo Paola   Gargiulo Sara   Cusano Roberto   Bruno William   Gliori Sara   Sertoli Mario R.   Burroni Anna   Savarino Vincenzo   Gensini Francesca   Sestini Roberta   Queirolo Paola   Goldstein Alisa M.   Scarrà Giovanna Bianchi  

Human Molecular Genetics, Vol. 15, Iss. 18, 2006-09 ,pp. : 2682-2689

Oxford University Press

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Allele diversity and germline mutation at the insulin minisatellite

By Stead John D.H.   Jeffreys Alec J.  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 713-723

Oxford University Press

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A large MSH2 Alu insertion mutation causes HNPCC in a German kindred

By Kloor Matthias   Sutter Christian   Wentzensen Nicolas   Cremer Friedrich   Buckowitz Annick   Keller Monika   Knebel Doeberitz Magnus   Gebert Johannes  

Human Genetics, Vol. 115, Iss. 5, 2004-10 ,pp. : 432-438

Springer Publishing Company

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Exclusion of a germline mutation in a classic Li-Fraumeni syndrome family

By Evans Susan C.   Mims Betsy   McMasters Kelly M.   Foster Carolyn J.   deAndrade Mariza   Amos Christopher I.   Strong Louise C.   Lozano Guillermina  

Human Genetics, Vol. 102, Iss. 6, 1998-07 ,pp. : 681-686

Springer Publishing Company

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