Familial occurrence of hemifacial microsomia with radial limb defects
โ Scribed by Moeschler, John ;Clarren, Sterling K. ;Opitz, John M.
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 313 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract ## BACKGROUND Severe anomalies of the forebrain together with radial limb anomalies have been reported in Steinfeld syndrome, XK aprosencephaly, and partial monosomy 13q. Steinfeld syndrome is an extremely variable autosomal dominant condition that, in severe cases, is characterized by
## Abstract Two families were investigated for the occurrence of IgA deficiency and antibodies to IgA. Several members of the families were found to be deficient for IgA1, as well as for IgA2, which strongly suggested that the disorder is genetically determined. By means of typing for genetic marke