The oto-palato-digital syndrome (OPD) is a rare X-linked disease with diagnostic skeletal features, conduction deafness, cleft palate and mild mental retardation. Differences in clinical presentation between families have led investigators to classify OPD into two subtypes: type I and type II. A lin
โฆ LIBER โฆ
Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28)
โ Scribed by Hoar, David I. ;Field, L. Leigh ;Beards, Francis ;Hoganson, George ;Rollnick, Beverly ;Hoo, Joe J.
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 195 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Oto-palato-digital syndrome type I: furt
โ
V. Biancalana; B. Marec; S. Odent; J. A. M. J. Hurk; A. Hanauer
๐
Article
๐
1991
๐
Springer
๐
English
โ 274 KB
Regional localization of a gene for nons
โ
Claes, Stephan; Volcke, Philippe; Devriendt, Koenraad; Holvoet, Maureen; Raeymae
๐
Article
๐
1999
๐
John Wiley and Sons
๐
English
โ 71 KB
๐ 1 views
Two families with nonspecific X-linked mental retardation (MRX) are presented. In the first family, MRX51, three male patients showed mild to borderline mental retardation. Multipoint linkage analysis yielded a maximal LOD score of 2.10 between markers DXS8012 and DXS1003, localizing the MRX51 gene