Polymicrogyria is an uncommon manifestation in 22q11.2 deletion syndrome
- 4 September 2000
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 94 (1) , 77-78
- https://doi.org/10.1002/1096-8628(20000904)94:1<77::aid-ajmg16>3.0.co;2-v
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Polymicrogyria in chromosome 22 deletion syndromeNeurology, 1998
- Enlarged sylvian fissures in infants with interstitial deletion of chromosome 22q11American Journal of Medical Genetics, 1997
- Cerebellar Hypoplasia in a Patient with Velo‐Cardio‐Facial SyndromeDevelopmental Medicine and Child Neurology, 1996
- Cerebellar atrophy in a patient with velocardiofacial syndrome.Journal of Medical Genetics, 1995
- Brain anomalies in velo‐cardio‐facial syndromeAmerican Journal of Medical Genetics, 1994
- Velo‐cardio‐facial syndrome presenting as holoprosencephalyClinical Genetics, 1985