Microgyria in the Distribution of the Middle Cerebral Artery in a Patient With DiGeorge Syndrome
- 1 November 1996
- journal article
- case report
- Published by SAGE Publications in Journal of Child Neurology
- Vol. 11 (6), 494-497
- https://doi.org/10.1177/088307389601100619
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Velo‐cardio‐facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 regionAmerican Journal of Medical Genetics, 1994
- Brain anomalies in velo-cardio-facial syndromeAmerican Journal of Medical Genetics, 1994
- DiGeorge syndrome: an historical review of clinical and cytogenetic features.Journal of Medical Genetics, 1993
- Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovariesAmerican Journal of Medical Genetics, 1993
- Decrease in thyrocalcitonin‐containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anamalyAmerican Journal of Medical Genetics, 1993
- Velo‐cardio‐facial syndrome: A review of 120 patientsAmerican Journal of Medical Genetics, 1993
- Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephalyAmerican Journal of Medical Genetics, 1989
- The DiGeorge anomaly as a developmental field defectAmerican Journal of Medical Genetics, 1986
- Spectrum of the DiGeorge “syndrome”The Journal of Pediatrics, 1980
- The spectrum of the DiGeorge syndromeThe Journal of Pediatrics, 1979