Pachygyria and cerebellar hypoplasia in a patient with a 2q22‐q23 deletion that includes the ZFHX1B gene
- 26 November 2003
- journal article
- other
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 127A (1) , 109
- https://doi.org/10.1002/ajmg.a.20607
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Pachygyria and cerebellar hypoplasia in Goldberg–Shprintzen syndromeAmerican Journal of Medical Genetics Part A, 2003
- “Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc finger homeo box 1B geneAmerican Journal of Medical Genetics, 2002
- Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline StructuresAmerican Journal of Human Genetics, 2001