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Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.
Bijlsma, E K; Gijsbers, A C J; Schuurs-Hoeijmakers, J H M; van Haeringen, A; Fransen van de Putte, D E; Anderlid, B-M; Lundin, J; Lapunzina, P; Pérez Jurado, L A; Delle Chiaie, B; Loeys, B; Menten, B; Oostra, A; Verhelst, H; Amor, D J; Bruno, D L; van Essen, A J; Hordijk, R; Sikkema-Raddatz, B; Verbruggen, K T; Jongmans, M C J; Pfundt, R; Reeser, H M; Breuning, M H; Ruivenkamp, C A L.
Affiliation
  • Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands. e.k.bijlsma@lumc.nl
Eur J Med Genet ; 52(2-3): 77-87, 2009.
Article in En | MEDLINE | ID: mdl-19306953
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Chromosomes, Human, Pair 16 / Chromosome Deletion / Intellectual Disability Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2009 Document type: Article Affiliation country: Países Bajos Country of publication: Países Bajos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Chromosomes, Human, Pair 16 / Chromosome Deletion / Intellectual Disability Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2009 Document type: Article Affiliation country: Países Bajos Country of publication: Países Bajos