Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly
Journal Articles
- Overview
- Research
- Identity
- Additional Document Info
- View All
Overview
status
publication date
- April 1, 2005
has subject area
- 06 Biological Sciences (FoR)
- 11 Medical and Health Sciences (FoR)
- Abnormalities, Multiple (MeSH)
- Child (MeSH)
- Child, Preschool (MeSH)
- Chromosome Deletion (MeSH)
- Chromosomes, Human, Pair 9 (MeSH)
- Craniofacial Abnormalities (MeSH)
- Cytogenetics (MeSH)
- Genetics & Heredity (Science Metrix)
- Genotype (MeSH)
- Humans (MeSH)
- In Situ Hybridization, Fluorescence (MeSH)
- Infant (MeSH)
- Language Development Disorders (MeSH)
- Microcephaly (MeSH)
- Phenotype (MeSH)
- Syndrome (MeSH)
published in
- Journal of Medical Genetics Journal