Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infant.

Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infant. Am J Med Genet A. 2012 Jun; 158A(6):1411-3.

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subject areas

Cardiomyopathy, Hypertrophic
Fatal Outcome
Fetal Distress
Humans
Infant
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases
Intracellular Signaling Peptides and Proteins
Male
Mutation
Noonan Syndrome

authors with profiles

Rebecca Hoban