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The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
Fujimoto M, Kantaputra PN, Ikegawa S, Fukushima Y, Sonta S, Matsuo M, Ishida T, Matsumoto T, Kondo S, Tomita H, Deng HX, D'urso M, Rinaldi MM, Ventruto V, Takagi T, Nakamura Y, Niikawa N. Fujimoto M, et al. Among authors: rinaldi mm. J Hum Genet. 1998;43(1):32-6. doi: 10.1007/s100380050033. J Hum Genet. 1998. PMID: 9609995
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity.
de Crecchio G, Simonelli F, Nunziata G, Mazzeo S, Greco GM, Rinaldi E, Ventruto V, Ciccodicola A, Miano MG, Testa F, Curci A, D'Urso M, Rinaldi MM, Cavaliere ML, Castelluccio P. de Crecchio G, et al. Among authors: rinaldi e, rinaldi mm. Clin Genet. 1998 Oct;54(4):315-20. doi: 10.1034/j.1399-0004.1998.5440409.x. Clin Genet. 1998. PMID: 9831343
Ring (13),t(2;6) associated with familial fragile (16).
Ventruto V, Rinaldi A, Renda S, Stabile M, Rinaldi MM, Cavaliere ML, Conte N, Aveta V. Ventruto V, et al. Among authors: rinaldi a, rinaldi mm. J Med Genet. 1984 Jun;21(3):233. doi: 10.1136/jmg.21.3.233. J Med Genet. 1984. PMID: 6748026 Free PMC article. No abstract available.
Clinical features of monosomy 10qter.
Zatterale A, Pagano L, Fioretti G, Caniglia M, Festa B, Renda S, Rinaldi MM, Ventruto V. Zatterale A, et al. Among authors: rinaldi mm. Ann Genet. 1983;26(2):106-8. Ann Genet. 1983. PMID: 6604483
Phenotypic variability in the chromosome 9 ring.
Cavaliere ML, Rinaldi MM, Castelluccio P, Cioffi C, Vendemmia M, Vendemmia S. Cavaliere ML, et al. Among authors: rinaldi mm. Acta Biomed Ateneo Parmense. 1997;68 Suppl 1:85-9. Acta Biomed Ateneo Parmense. 1997. PMID: 10021722 Review.
30 results