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Hindustani, the lingua franca of Northern India and Pakistan, has two standardised registers: Hindi and Urdu.Grammatical differences between the two standards are minor but each uses its own script: Hindi uses Devanagari while Urdu uses an extended form of the Perso-Arabic script, typically in the Nastaʿlīq style.
Language disorders or language impairments are disorders that involve the processing of linguistic information. Problems that may be experienced can involve grammar (syntax and/or morphology), semantics (meaning), or other aspects of language. These problems may be receptive (involving impaired language comprehension), expressive (involving ...
Schwa deletion, or schwa syncope, is a phenomenon that sometimes occurs in Assamese, Hindi, Urdu, Bengali, Kashmiri, Punjabi, Gujarati, and several other Indo-Aryan languages with schwas that are implicit in their written scripts.
Hypochondria is an old concept whose meaning has repeatedly changed over its lifespan. [1] It has been claimed that this debilitating condition results from an inaccurate perception of the condition of body or mind despite the absence of an actual medical diagnosis. [2] An individual with hypochondriasis is known as a hypochondriac.
Standard Hindi (also High Hindi, Manak Hindi) is the language of the government and is one of the official languages of India, Standard Urdu is the state language and national language of Pakistan, Dakhini is the historical literary dialect of the Deccan region, and Rekhta the "mixed" Hindustani of medieval poetry. [12]
This is the pronunciation key for IPA transcriptions of Hindi and Urdu on Wikipedia. It provides a set of symbols to represent the pronunciation of Hindi and Urdu in Wikipedia articles, and example words that illustrate the sounds that correspond to them.
Hindi–Urdu transliteration (or Hindustani transliteration) is essential for Hindustani speakers to understand each other's text, and it is especially important considering that the underlying language of both the Hindi & Urdu registers are almost the same. [4]
Hypervalinemia has an autosomal recessive pattern of inheritance.. Hypervalinemia is inherited in an autosomal recessive manner. [1] This means the defective gene responsible for the disorder is located on an autosome, and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder.