बहुमंज़ि इसके अंग्रेजी अर्थ का उदाहरण

In 2003, Square Enix began a drive to begin developing "polymorphic content", a marketing and sales strategy to "[provide] well-known properties on several platforms, allowing exposure of the products to as wide an audience as possible".

In early 2005, Square Enix announced a "World of Mana" project, the application of this "polymorphic content" idea to the Mana franchise, which would include several games across different genres and platforms.

Histopathological changes are that of a chronic granulomatous disorder, characterized by fibrinoid necrosis, infiltration by polymorphonuclear cells, lymphocytes, plasma cells and macrophages.

The 64bit Java Virtual Machine which allows supports development in both Java and Magik (an object-oriented programming language that supports multiple inheritance, polymorphism, multi-threading and is dynamically typed).

Elektra Records singles Magik is an object-oriented programming language that supports multiple inheritance and polymorphism, and it is dynamically typed.

Scott encoding can be done in untyped lambda calculus, whereas its use with types requires a type system with recursion and type polymorphism.

" He was particularly harsh in his denunciation of sexual ambiguity and polymorphous androgyny in the book.

This releases cytokines that recruit polymorphonuclear cells (PMN) to the sub-mucosa.

Most PMs have an autosomal recessive polymorphism in the CYP2D6 locus which results in the severely compromised metabolism of at least 25 drugs.

It is believed that there are hundreds of potential polymorphism which will result in a PM, some result in functionally deficient CYP2D6, while others cause the absence of CYP2D6.

Of the five mutations described by Heiss and colleagues in Nature Genetics, four were single nucleotide polymorphisms all resulting in the change of highly conserved amino acids.

In two of these families, two family-specific single nucleotide polymorphisms were present while in the other there persisted a large-scale deletion (821 base pairs of DNA) on chromosome 3 which includes 74 bases coding for a section of the H/ACA domain.

These mutations are also autosomal recessive with three specific single-nucleotide polymorphisms being recognized which result in dyskeratosis congenita.