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Structure: Internal structure identifier : 300073

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

Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases

S. Baer , A. Afenjar , T. Smol , A. Piton , B. Gérard et al.
Clinical Genetics, 2018, 94 (1), pp.141-152. ⟨10.1111/cge.13254⟩
Journal articles hal-02393652v1
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Use of magnetic resonance image registration to estimate displacement in the human earcanal due to the insertion of in-ear devices

Simon Benacchio , Olivier Doutres , Arthur Varoquaux , Eric Wagnac , Arnaud Le Troter et al.
Journal of the Acoustical Society of America, 2019, 146 (4), pp.2452-2465. ⟨10.1121/1.5126857⟩
Journal articles hal-02370631v1

Vox Sanguinis International Forum on donor notification and counselling strategies for markers of transfusion-transmissible infections: summary

R. Sharma , M. Lozano , M. Fearon , M. Bigham , R. Djoudi et al.
Vox Sanguinis, 2016, 54 (2), pp.289-95. ⟨10.1111/vox.12469⟩
Journal articles hal-01496350v1