Coffin Lowry Syndrome Karyotype
Sept. 13, 2024
Coffin-Lowry phenotype in a patient with a complex chromosome rearrangement | Journal of Medical Genetics Coffin-Lowry syndrome: clinical and molecular features | 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 | European Journal of Human Genetics 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
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