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Author Details
Full Name
Marijcke W M Veltman
Affiliation
University of Cambridge
ORCID
Career Start Year
2000
Papers
12
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
27899602
The Human Phenotype Ontology in 2017.
Nucleic Acids Res
2017
16470730
Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13.
Am J Med Genet A
2006
15796127
A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study.
J Autism Dev Disord
2005
16178933
Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
J Child Psychol Psychiatry
2005
16314754
Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review.
Psychiatr Genet
2005
15952184
An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet
2005
14991431
Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.
Eur Child Adolesc Psychiatry
2004
15576546
Effect on health-related outcomes of interventions to alter the interaction between patients and practitioners: a systematic review of trials.
Ann Fam Med
2004
15318025
Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders.
Psychiatr Genet
2004
12843333
A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype.
J Med Genet
2003
11803514
The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.
Am J Med Genet
2001
11075693
An evaluation of favorite kind of day drawings from physically maltreated and non-maltreated children.
Child Abuse Negl
2000
1 - 12 of 12
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