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February 1, 2008PEDIATRICS

Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation

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Authors

ABAgatino BattagliaUniversity College DublinHHH. Eugene HoymeSanford HealthBDBruno DallapiccolaUniversity of Siena

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Cite This Study

Battaglia et al. (2008) studied this question.

synapsesocial.com/papers/6a99e3b9c74394daee3fd3aahttps://doi.org/10.1542/peds.2007-0929
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation2001 · 63 citations
  2. 2Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.1995 · 59 citations
  3. 3Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions1999 · 105 citations
  4. 4Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.32000 · 32 citations