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July 1, 1995Journal of Medical GeneticsOpen Access

Cerebellar atrophy in a patient with velocardiofacial syndrome.

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Authors

DLDavid R. LynchDMDonna M. McDonald‐McGinnEZElaine H. Zackai

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Cite This Study

Lynch et al. (1995) studied this question.

synapsesocial.com/papers/6a96e0ccdbc641e6a0a6e65dhttps://doi.org/10.1136/jmg.32.7.561
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.1993 · 489 citations
  2. 2The Velo-Cardio-Facial Syndrome: A Clinical and Genetic Analysis1981 · 297 citations
  3. 3Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q111993 · 181 citations
  4. 4Velo‐cardio‐facial syndrome: A review of 120 patients1993 · 432 citations
  5. 5Brain anomalies in velo‐cardio‐facial syndrome1994 · 131 citations