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February 11, 2008American Journal of Medical Genetics Part A

Congenital heart defects in spinal muscular atrophy type I: A clinical report of two siblings and a review of the literature

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Authors

LMLeonie A. MenkeEmma KinderziekenhuisBPBwee Tien Poll‐TheAmsterdam University Medical CentersSCSally‐Ann B. ClurPediatric Cardiology

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Menke et al. (2008) studied this question.

synapsesocial.com/papers/6a9715f90f79e4f014b32082https://doi.org/10.1002/ajmg.a.32233
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  1. 1Acutely altered hemodynamics following venous obstruction in the early chick embryo2003 · 61 citations
  2. 2Clinical Spectrum and Diagnostic Criteria of Infantile Spinal Muscular Atrophy: Further Delineation on the Basis of SMN Gene Deletion Findings1996 · 124 citations
  3. 3A hungarian study on Werdnig-Hoffmann disease.1989 · 77 citations
  4. 4The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy1998 · 155 citations