Microdeletion syndrome
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- The Presence of Two Rare Genomic Syndromes, 1Q21 Deletion and Xq28 Duplication, Segregating Independently in a Family with Intellectual Disability
- 9P24 Triplication and 15Q13 Deletion in Syndromic Hydrocephalus with Diffuse Villous Hyperplasia of the Choroid Plexus
- About the Prenatalsafe® Prenatal Test the Prenatalsafe® Non-Invasive Prenatal Test (NIPT) Looks at the DNA (Genetic Material) in Your Blood
- Prenatal Detection of Unbalanced Chromosomal Rearrangements by Array-CGH
- 7Q35 Microdeletion and 15Q13.3 and Xp22.33 Microduplications in A
- Proximal Microdeletions and Microduplications of 1Q21.1 Contribute to Variable Abnormal Phenotypes
- 2Q23.1 Microdeletion Syndrome
- 15Q13.3 Microdeletion
- The 15Q11.2 BP1-BP2 Microdeletion
- 15Q Deletions FTNW
- Non-Invasive Prenatal Aneuploidies and Microdeletion Screening Test Report
- The Genetics of Microdeletion and Microduplication Syndromes: an Update
- Type 1 Established Condition List
- Chromosomal Basis of Human Diseases
- The Discovery of Microdeletion Syndromes in the Post-Genomic Era: Review of the Methodology and Characterization of a New 1Q41q42 Microdeletion Syndrome Lisa G
- Consequences of 22Q11.2 Microdeletion on the Genome, Individual and Population Levels
- Identification of Genomic Loci Contributing to Agenesis of the Corpus Callosum Mary C
- Chromosome 15