Detalhe da pesquisa
1.
The Human Phenotype Ontology in 2017.
Nucleic Acids Res
; 45(D1): D865-D876, 2017 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27899602
2.
Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review.
Psychiatr Genet
; 15(4): 243-54, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16314754
3.
A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study.
J Autism Dev Disord
; 35(1): 117-27, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15796127
4.
Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders.
Psychiatr Genet
; 14(3): 131-7, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15318025
5.
Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
J Child Psychol Psychiatry
; 46(10): 1089-96, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16178933
6.
Effect on health-related outcomes of interventions to alter the interaction between patients and practitioners: a systematic review of trials.
Ann Fam Med
; 2(6): 595-608, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15576546
7.
Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.
Eur Child Adolesc Psychiatry
; 13(1): 42-50, 2004 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-14991431