Coffin Lowry Syndrome Karyotype
Aug. 31, 2024
Coffin-Lowry phenotype in a patient with a complex chromosome rearrangement | Journal of Medical Genetics Familial co-segregation of Coffin–Lowry syndrome inherited from the mother and autosomal dominant Waardenburg type IV syndrome due to deletion of EDNRB inherited from the father - ScienceDirect Coffin-Lowry syndrome: clinical and molecular features | Journal of Medical Genetics Coffin-Lowry syndrome: clinical and molecular features | Journal of Medical Genetics | Coffin Lowry Syndrome Karyotype