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  2. Phocomelia - Wikipedia

    en.wikipedia.org/wiki/Phocomelia

    Phocomelia is a congenital condition that involves malformations of human arms and legs which result in a flipper-like appendage. [1] [2] A prominent cause of phocomelia is the mother being prescribed the use of the drug thalidomide during pregnancy; however, the causes of most cases are to be determined. [2]

  3. File:Phocomelia1.jpg - Wikipedia

    en.wikipedia.org/wiki/File:Phocomelia1.jpg

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  4. List of online digital musical document libraries - Wikipedia

    en.wikipedia.org/wiki/List_of_Online_Digital...

    Printable sheet music primarily for singers and voice teachers—most downloadable. Emphasis on standard classical and traditional repertoire. IPA transcriptions available for every German, French, Italian and Latin song in the index. Supplementary information on more than 250 songs. ART SONG CENTRAL: The Ashford Sheet Music Collection

  5. Dysmelia - Wikipedia

    en.wikipedia.org/wiki/Dysmelia

    external causes during pregnancy (thus not inherited), e.g. via amniotic band syndrome; teratogenic drugs (e.g. thalidomide, which causes phocomelia) or environmental chemicals; ionizing radiation (nuclear weapons, radioiodine, radiation therapy) infections; metabolic imbalance

  6. Ectrodactyly - Wikipedia

    en.wikipedia.org/wiki/Ectrodactyly

    The cause of cleft hand lies, for what is known, partly in genetics. The inheritance of cleft hand is autosomal dominant and has a variable penetrance of 70%. [6] Cleft hand can be a spontaneous mutation during pregnancy (de novo mutation). The exact chromosomal defect in isolated cleft hand is not yet defined.

  7. Category:Phocomelia - Wikipedia

    en.wikipedia.org/wiki/Category:Phocomelia

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  8. File:Ears of phocomelia patients.jpg - Wikipedia

    en.wikipedia.org/wiki/File:Ears_of_phocomelia...

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  9. Roberts syndrome - Wikipedia

    en.wikipedia.org/wiki/Roberts_syndrome

    Roberts syndrome, or sometimes called pseudothalidomide syndrome, is an extremely rare autosomal recessive genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, and legs.