7 top medical experts on Chromosome 19q13.11 Deletion Syndrome across 0 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Chromosome 19q13.11 Deletion Syndrome: The 19q13.11 microdeletion is characterized by several major features including pre and postnatal growth retardation, slender habitus, severe postnatal feeding difficulties, microcephaly, intellectual deficit with speech disturbance, hypospadias and ectodermal dysplasia presented by scalp aplasia, thin and sparse hair, eyebrows and eyelashes, thin and dry skin and dysplasic nails.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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