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Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay.
- Source :
-
American journal of medical genetics. Part A [Am J Med Genet A] 2014 Nov; Vol. 164A (11), pp. 2964-7. Date of Electronic Publication: 2014 Aug 14. - Publication Year :
- 2014
- Subjects :
- Child, Preschool
Comparative Genomic Hybridization
Craniofacial Abnormalities diagnosis
Facies
Humans
Language Development Disorders diagnosis
Male
Phenotype
Syndrome
Chromosome Duplication
Chromosomes, Human, Pair 7
Craniofacial Abnormalities genetics
Language Development Disorders genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1552-4833
- Volume :
- 164A
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics. Part A
- Publication Type :
- Report
- Accession number :
- 25124455
- Full Text :
- https://doi.org/10.1002/ajmg.a.36715