TY  - JOUR
T1  - Genetics of Radial Deficiencies
AU  - de Graaff, Esther
AU  - Kozin, Scott H.
Y1  - 2009/07/01
N1  - 10.2106/JBJS.I.00073
JO  - The Journal of Bone & Joint Surgery
SP  - 81
EP  - 86
VL  - 91
IS  - Supplement_4
N2  - 
More than 15% of the anomalies described in the London Dysmorphology Database are associated with various manifestations of radial longitudinal deficiency1. Their etiology may be genetic, environmental, or a combination of these factors. While most of the known inherited disorders are single-gene disorders, family members carrying the same mutation often show a range of phenotypes. This indicates that other genes and/or the environment play a large role in the phenotypic variability of radial longitudinal deficiency.

SN  - 0021-9355
M3  - doi: 10.2106/JBJS.I.00073
UR  - http://dx.doi.org/10.2106/JBJS.I.00073
ER  -