Refined mapping of the gene for otopalatodigital syndrome type I: Figure 1

作者：Tomoki Kosho, T Uemura, M Tanimura, H Ohashi, K Muroya, T Ogata · 发表于：Journal of Medical Genetics · 年份：2002 · DOI：10.1136/jmg.39.2.e7 · 被引用次数：4 · 研究领域：Genomic variations and chromosomal abnormalities、Congenital limb and hand anomalies、Congenital Ear and Nasal Anomalies

In summary, the present study suggests that the OPD-I critical region is further narrowed down from the ∼12 Mb region distal to DXS539 to the ∼6 Mb region between DXS8011 and DXS1108, with a combined maximum lod score of 4.09.Further studies will permit a better localisation of the gene for OPD-I.. . . . .