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Description
  • Holoprosencephaly is a heterogenous group of diseases. It is caused by full or partial lack of separatio of the embryonic prosencephalon into two different hemisfere. It may by associated with malformations in the central part of the face. It is often caused by the mothers explosure to teratogens in the first weeks of pregnancy or chromosomal abberationions. Hereditary holoprosencephalies are described as autosomal dominant diseases with varied penetration or autosomal recessive or X-linked syndromes.
  • Holoprosencephaly is a heterogenous group of diseases. It is caused by full or partial lack of separatio of the embryonic prosencephalon into two different hemisfere. It may by associated with malformations in the central part of the face. It is often caused by the mothers explosure to teratogens in the first weeks of pregnancy or chromosomal abberationions. Hereditary holoprosencephalies are described as autosomal dominant diseases with varied penetration or autosomal recessive or X-linked syndromes. (en)
Title
  • Family case of holoprosencephaly
  • Family case of holoprosencephaly (en)
skos:prefLabel
  • Family case of holoprosencephaly
  • Family case of holoprosencephaly (en)
skos:notation
  • RIV/00216224:14110/14:00077713!RIV15-MSM-14110___
http://linked.open...avai/riv/aktivita
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  • I
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 16447
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  • RIV/00216224:14110/14:00077713
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  • holoprosencephaly (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...ontrolniKodProRIV
  • [E090E61F39A0]
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http://linked.open...UplatneniVysledku
http://linked.open...iv/tvurceVysledku
  • Ventruba, Pavel
  • Vlašínová, Iva
  • Gerychová, Romana
  • Grochová, Ilga
http://localhost/t...ganizacniJednotka
  • 14110
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