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Molecular diagnosis of microcephaly and pontocerebellar hypoplasia (NGS screening panel: 71 genes)

  • Phone : 49 (0)7071 565 44 55
  • Additional Phone : -
  • Fax : 49 (0)7071 565 44 22
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Last update: August 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.