224 top medical experts on Chromosome 1p36 Deletion Syndrome across 26 countries and 22 U.S. states, including 50 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Chromosome 1p36 Deletion Syndrome: A rare chromosomal anomaly characterized by distinctive facial dysmorphic features, hypotonia, developmental delay, intellectual disability, seizures, heart defects, poor/absent speech, and prenatal onset growth deficiency.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: 1p36 deletion syndrome,  1p36.33 deletion,  1p36 deletion syndrome Chromosome 1,  Deletion 1p36.33,  Monosomy 1p36 syndrome


  

        

                    


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