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Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.
J Intern Med. 1998 Jun;243(6):515-20. doi: 10.1046/j.1365-2796.1998.00332.x.
J Intern Med. 1998.
PMID: 9681852
Free article.
A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.
Seri M, Celli I, Betsos N, Claudiani F, Camera G, Romeo G.
Seri M, et al. Among authors: betsos n.
Clin Genet. 1997 Feb;51(2):86-90. doi: 10.1111/j.1399-0004.1997.tb02425.x.
Clin Genet. 1997.
PMID: 9111993
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Double heterozygosity for a RET substitution interfering with splicing and an EDNRB missense mutation in Hirschsprung disease.
Auricchio A, Griseri P, Carpentieri ML, Betsos N, Staiano A, Tozzi A, Priolo M, Thompson H, Bocciardi R, Romeo G, Ballabio A, Ceccherini I.
Auricchio A, et al. Among authors: betsos n.
Am J Hum Genet. 1999 Apr;64(4):1216-21. doi: 10.1086/302329.
Am J Hum Genet. 1999.
PMID: 10090908
Free PMC article.
No abstract available.
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HOX11L1, a gene involved in peripheral nervous system development, maps to human chromosome 2p13.1-->p12 and mouse chromosome 6C3-D1.
Puliti A, Cinti R, Betsos N, Romeo G, Ceccherini I.
Puliti A, et al. Among authors: betsos n.
Cytogenet Cell Genet. 1999;84(1-2):115-7. doi: 10.1159/000015234.
Cytogenet Cell Genet. 1999.
PMID: 10343123
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