## Abstract Since the discovery of the first gene causing holoprosencephaly (HPE), over 500 patients with mutations in genes associated with non‐chromosomal, non‐syndromic HPE have been described, with detailed descriptions available in over 300. Comprehensive clinical analysis of these individuals
Genotype–phenotype analysis of human frontoparietal polymicrogyria syndromes
✍ Scribed by Xianhua Piao; Bernard S. Chang; Adria Bodell; Katelyn Woods; Bruria BenZeev; Meral Topcu; Renzo Guerrini; Hadassa Goldberg-Stern; Laszlo Sztriha; William B. Dobyns; A. James Barkovich; Christopher A. Walsh
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 216 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0364-5134
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