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February 1, 2001Journal of Medical GeneticsOpen Access

Use 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 retardation

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Authors

FGF GiraudeauLTLaurence TaineCentre Hospitalier Universitaire de BordeauxVBValérie BiancalanaCentre Hospitalier Universitaire de Lille

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Giraudeau et al. (2001) studied this question.

synapsesocial.com/papers/6a99e41f819ffb2fe2b4f013https://doi.org/10.1136/jmg.38.2.121
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: Cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection1997 · 25 citations
  2. 2A rapid method for the purification of DNA from blood1987 · 321 citations
  3. 3Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome1995 · 53 citations