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Volumn 50, Issue 4, 2008, Pages 243-
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Genetic neurodevelopmental diseases - How well do we know them?
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Author keywords
[No Author keywords available]
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Indexed keywords
FRAGILE X MENTAL RETARDATION PROTEIN;
METHYL CPG BINDING PROTEIN 2;
AUTISM;
DEVELOPMENTAL DISORDER;
EDITORIAL;
FLUORESCENCE IN SITU HYBRIDIZATION;
FRAGILE X SYNDROME;
GENE IDENTIFICATION;
GENETIC DATABASE;
GENETIC DISORDER;
HAPPY PUPPET SYNDROME;
HEALTH EDUCATION;
HUMAN;
KARYOTYPING;
MENTAL DEFICIENCY;
NEUROLOGIC DISEASE;
PEDIATRIC REHABILITATION;
PRIORITY JOURNAL;
RETT SYNDROME;
X LINKED MENTAL RETARDATION;
CHILD;
CHILD DEVELOPMENT DISORDERS, PERVASIVE;
GENETIC MARKERS;
GENETIC SCREENING;
GENOTYPE;
HUMANS;
MENTAL RETARDATION;
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EID: 41149136792
PISSN: 00121622
EISSN: 14698749
Source Type: Journal
DOI: 10.1111/j.1469-8749.2008.00243.x Document Type: Editorial |
Times cited : (1)
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References (5)
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