Background: The rare association between NSGCT and AMKL has been reported since 1985.1,2 Isochromosome 12p is the most common cytogenetic abnormality in but only rarely found unless with NSGCT.3 Case Presentation: A 31-year-old male presented pancytopenia on background of a both mediastinal fibrolamellar hepatocellular carcinoma diagnosed 5 months prior. Circulating blasts cytoplasmic blebbing ...

A case of trisomy 14q mosaicism is described and compared with three other similar reported cases. The clinical picture is characterised by severe developmental retardation, failure to thrive, and somatic abnormalities including skeletal asymmetry, high arched or cleft palate, and low set dysplastic ears. The present chromosome imbalance probably resulted from dissociation of a balanced 14q15q ...

In this work, the initial anisotropy and its evolution with strain, hardening and rupture of DC04 mild steel are characterized by using (i) a phenomenological constitutive model composed by the non-quadratic Yld2004-18p yield criterion combined with an isotropic hardening law and (ii) a macroscopic rupture criterion. For this purpose, an inverse methodology of material parameters identification...

A mosaic karyotype 46,XX,del(18)(p11)/46,XX,-18,+?i(18q) was found in cultured amniotic cells. Fetal blood sampling confirmed the presence of both cell lines. The pregnancy was terminated and the two cell lines were demonstrated in varying proportions in the fetal tissues. The few abnormal features seen in the fetus may represent a mild expression of the 18p-- phenotype inhibiting the effects o...