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J Halley

Showing results (81-90 of 194) with videos related to

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Pediatric Neurology|July 5, 2011
A novel GPR56 mutation causes bilateral frontoparietal polymicrogyriaRong Luo, Hye Min Yang, Zhaohui Jin, et al.
Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
Human Genetics|October 19, 2004
The CLCA gene locus as a modulator of the gastrointestinal basic defect in cystic fibrosisMargit Ritzka, Frauke Stanke, Silke Jansen, et al.
Neurogenetics|April 23, 2009
Movement disorder and neuronal migration disorder due to ARFGEF2 mutationM C Y de Wit, I F M de Coo, D J J Halley, et al.
Journal of Medical Genetics|July 5, 2003
FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaicsB B A de Vries, L-A Severijnen, A Jacobs, et al.
Carbohydrate Polymers|September 8, 2015
Lubrication of starch in ionic liquid-water mixtures: Soluble carbohydrate polymers form a boundary film on hydrophobic surfacesGleb E Yakubov, Lei Zhong, Ming Li, et al.
American Journal of Medical Genetics|September 1, 1991
DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.
Physical Chemistry Chemical Physics : PCCP|April 23, 2015
Understanding the structural disorganization of starch in water-ionic liquid solutionsBinjia Zhang, Ling Chen, Fengwei Xie, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 13, 2013
Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature reviewIbrahim Tanyalçin, Helene Verhelst, Dicky J J Halley, et al.
Human Genetics|December 18, 1998
Screening with the FMR1 protein test among mentally retarded malesB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Pageof 20

Showing results (81-90 of 194) with videos related to

Sort By:
Pageof 20
Pediatric Neurology|July 5, 2011
A novel GPR56 mutation causes bilateral frontoparietal polymicrogyriaRong Luo, Hye Min Yang, Zhaohui Jin, et al.
Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
Human Genetics|October 19, 2004
The CLCA gene locus as a modulator of the gastrointestinal basic defect in cystic fibrosisMargit Ritzka, Frauke Stanke, Silke Jansen, et al.
Neurogenetics|April 23, 2009
Movement disorder and neuronal migration disorder due to ARFGEF2 mutationM C Y de Wit, I F M de Coo, D J J Halley, et al.
Journal of Medical Genetics|July 5, 2003
FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaicsB B A de Vries, L-A Severijnen, A Jacobs, et al.
Carbohydrate Polymers|September 8, 2015
Lubrication of starch in ionic liquid-water mixtures: Soluble carbohydrate polymers form a boundary film on hydrophobic surfacesGleb E Yakubov, Lei Zhong, Ming Li, et al.
American Journal of Medical Genetics|September 1, 1991
DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.
Physical Chemistry Chemical Physics : PCCP|April 23, 2015
Understanding the structural disorganization of starch in water-ionic liquid solutionsBinjia Zhang, Ling Chen, Fengwei Xie, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 13, 2013
Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature reviewIbrahim Tanyalçin, Helene Verhelst, Dicky J J Halley, et al.
Human Genetics|December 18, 1998
Screening with the FMR1 protein test among mentally retarded malesB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Pageof 20