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Structure: Internal structure identifier : 97656

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.

F Giraudeau , L Taine , V Biancalana , B Delobel , H Journel et al.
Journal of Medical Genetics, 2001, 38 (2), pp.121-5. ⟨10.1136/jmg.38.2.121⟩
Journal articles hal-01158343v1