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, 2013 Il contributo offre una rassegna competa, ordinata e ragionata delle decisioni giurisprudenziali, costituzionali ed ordinarie, sull'art. 271 c.p.p.
CAMON, ALBERTO
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Journal of Paediatrics and Child Health, 1972
SYNOPSISThe cytogenic findings in 271 mongols are described and discussed. The cases were ascertained by routine referral and also by total ascertainment studies of institutionalised mongols. 23 of the 271 did not have regular mongol karyotypes. It is suggested that all mongols should be referred for chromosomal studies.
G R, Sutherland, S, Wiener
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SYNOPSISThe cytogenic findings in 271 mongols are described and discussed. The cases were ascertained by routine referral and also by total ascertainment studies of institutionalised mongols. 23 of the 271 did not have regular mongol karyotypes. It is suggested that all mongols should be referred for chromosomal studies.
G R, Sutherland, S, Wiener
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, 2017 Il contributo propone una rassegna ordinata delle decisioni giurisprudenziali sull'art. 271 c.p.p.
Alberto Camon
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Neuromuscular Disorders, 2014
Mutations affecting skeletal muscle isoforms of the tropomyosin genes may cause nemaline myopathy (NM), cap myopathy, core-rod myopathy, congenital fibre-type disproportion, core-rod myopathy, distal arthrogryposes and Escobar syndrome. Here we correlate the clinical picture of these diseases with novel (16) and previously reported (31) mutations of ...
M. Marttila +39 more
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Mutations affecting skeletal muscle isoforms of the tropomyosin genes may cause nemaline myopathy (NM), cap myopathy, core-rod myopathy, congenital fibre-type disproportion, core-rod myopathy, distal arthrogryposes and Escobar syndrome. Here we correlate the clinical picture of these diseases with novel (16) and previously reported (31) mutations of ...
M. Marttila +39 more
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2021
Il contributo offre una rassegna ragionata della giurisprudenza in materia di divieti di utilizzazione delle ...
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Il contributo offre una rassegna ragionata della giurisprudenza in materia di divieti di utilizzazione delle ...
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Identification of the novel HLA‐DRB1*11:271 allele by next‐generation sequencing
Hla, 2021Sudan Tao, Ji He, Faming Zhu
exaly