Coffin Lowry Syndrome Karyotype
Nov. 28, 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
![PDF] Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomes. |…](https://d3i71xaburhd42.cloudfront.net/b2a4236a67320cb87ce96bbe7641f3784f2600b4/3-Figure1-1.png){kind=link}
:max_bytes(150000):strip_icc()/cute-boy-with-down-syndrome-playing-with-dad-on-in-home-1053058542-b676079901424e27b576af7d8f96dbd1.jpg){kind=link}
![PDF] Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomes. |…](https://d3i71xaburhd42.cloudfront.net/b2a4236a67320cb87ce96bbe7641f3784f2600b4/8-Figure6-1.png){kind=link}
:max_bytes(150000):strip_icc()/KabukiIllustration-2210ff2d7c6348bdaed11e3abfdcfa19.jpg){kind=link}
