Microcephalic osteodysplastic primordial short stature type II with café‐au‐lait spots and moyamoya disease: Another patient
- 27 January 2004
- journal article
- other
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 127A (2) , 218-220
- https://doi.org/10.1002/ajmg.a.20647
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Microcephalic osteodysplastic primordial short stature type II with cafe‐au‐lait spots and moyamoya diseaseAmerican Journal of Medical Genetics Part A, 2003
- Mapping of a Familial Moyamoya Disease Gene to Chromosome 3p24.2-p26American Journal of Human Genetics, 1999
- Ito hypomelanosis and moyamoya diseasePediatric Neurology, 1995
- Fanconi anemia and moyamoyaNeurology, 1995
- Vascular occlusion associated with incontinentia pigmentiPediatric Neurology, 1994