## Abstract Monosomy 1p36 is the most common terminal deletion syndrome seen in humans, occurring in ∼1 in 5,000 live births. Common features include mental retardation, characteristic dysmorphic features, hypotonia, seizures, hearing loss, heart defects, cardiomyopathy, and behavior abnormalities.
Distal 3p deletion syndrome: Detailed molecular cytogenetic and clinical characterization of three small distal deletions and review
✍ Scribed by Helena Malmgren; Sigrid Sahlén; Katarina Wide; Mikael Lundvall; Elisabeth Blennow
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 222 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
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