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B C J Hamel

Showing results (11-20 of 23) with videos related to

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Neuropediatrics|April 4, 2002
MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findingsN Geerdink, J J Rotteveel, M Lammens, et al.
European Journal of Medical Genetics|March 1, 2006
Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literatureI Feenstra, D A Koolen, J Van der Pas, et al.
American Journal of Medical Genetics. Part A|March 23, 2005
Renpenning syndrome comes into focusRoger E Stevenson, C W Bennett, F Abidi, et al.
Clinical Genetics|June 26, 2002
De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastiaT Kleefstra, H G Yntema, A R Oudakker, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2011
Auditory change detection in fragile X syndrome males: a brain potential studyM J W Van der Molen, M W Van der Molen, K R Ridderinkhof, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 1, 2011
Auditory and visual cortical activity during selective attention in fragile X syndrome: a cascade of processing deficienciesM J W Van der Molen, M W Van der Molen, K R Ridderinkhof, et al.
Brain and Cognition|January 21, 2012
Attentional set-shifting in fragile X syndromeM J W Van der Molen, M W Van der Molen, K R Ridderinkhof, et al.
Clinical Genetics|May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in IndonesiaT I Winarni, F E P Mundhofir, A Ediati, et al.
Clinical Genetics|September 14, 2007
Pure subtelomeric microduplications as a cause of mental retardationE M Ruiter, D A Koolen, T Kleefstra, et al.
Clinical Genetics|September 10, 2004
Genotype-phenotype studies in three families with mutations in the polyglutamine-binding protein 1 gene (PQBP1)T Kleefstra, C E Franken, Y H J M Arens, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Neuropediatrics|April 4, 2002
MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findingsN Geerdink, J J Rotteveel, M Lammens, et al.
European Journal of Medical Genetics|March 1, 2006
Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literatureI Feenstra, D A Koolen, J Van der Pas, et al.
American Journal of Medical Genetics. Part A|March 23, 2005
Renpenning syndrome comes into focusRoger E Stevenson, C W Bennett, F Abidi, et al.
Clinical Genetics|June 26, 2002
De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastiaT Kleefstra, H G Yntema, A R Oudakker, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2011
Auditory change detection in fragile X syndrome males: a brain potential studyM J W Van der Molen, M W Van der Molen, K R Ridderinkhof, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 1, 2011
Auditory and visual cortical activity during selective attention in fragile X syndrome: a cascade of processing deficienciesM J W Van der Molen, M W Van der Molen, K R Ridderinkhof, et al.
Brain and Cognition|January 21, 2012
Attentional set-shifting in fragile X syndromeM J W Van der Molen, M W Van der Molen, K R Ridderinkhof, et al.
Clinical Genetics|May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in IndonesiaT I Winarni, F E P Mundhofir, A Ediati, et al.
Clinical Genetics|September 14, 2007
Pure subtelomeric microduplications as a cause of mental retardationE M Ruiter, D A Koolen, T Kleefstra, et al.
Clinical Genetics|September 10, 2004
Genotype-phenotype studies in three families with mutations in the polyglutamine-binding protein 1 gene (PQBP1)T Kleefstra, C E Franken, Y H J M Arens, et al.
Pageof 3