Molecular genetic analysis of infantile hypertrohpic pyloric stenosis
The aim of this study was to identify susceptibility genes for the common disease Infantile Hypertrophic Pyloric Stenosis (IHPS) using a whole genome screening approach. IHPS is a form of gastrointestinal obstruction with an incidence between 1 and 5 per 1000 live births. It is characterized by hype...
Main Author: | Georgoula, C. |
---|---|
Published: |
University College London (University of London)
2009
|
Subjects: | |
Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.625155 |
Similar Items
-
Molecular genetic analysis of paediatric low-grade astrocytoma
by: Tatevossian, R. G.
Published: (2010) -
Molecular genetic and cellular studies in childhood leukaemia
by: Samuel, David Ponniah
Published: (2008) -
Clinical and molecular characterisation of rare genetic syndromes with unknown aetiology
by: Teixeira Bernardo De Sousa, S. A.
Published: (2014) -
Clinical, genetic and molecular studies into hereditary renal tubular proteinuria
by: Issler, N.
Published: (2014) -
Auditory processing in the syndrome of infantile spasms
by: Werner, Klaus-Georg Erich
Published: (2007)