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Diagnostic strategy in segmentation defect of the vertebrae: a retrospective study of 73 patients.
J Med Genet. 2018 Jun;55(6):422-429. doi: 10.1136/jmedgenet-2017-104939. Epub 2018 Feb 19.
J Med Genet. 2018.
PMID: 29459493
Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency.
Perche O, Menuet A, Marcos M, Liu L, Pâris A, Utami KH, Kervran D, Cacheux V, Laudier B, Briault S.
Perche O, et al. Among authors: kervran d.
Eur J Med Genet. 2013 Nov;56(11):635-41. doi: 10.1016/j.ejmg.2013.07.007. Epub 2013 Sep 4.
Eur J Med Genet. 2013.
PMID: 24013099
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The new platelet alloantigen Cab a: a single point mutation Gln 716 His on the alpha 2 integrin.
Bertrand G, Jallu V, Saillant D, Kervran D, Martageix C, Kaplan C.
Bertrand G, et al. Among authors: kervran d.
Transfusion. 2009 Oct;49(10):2076-83. doi: 10.1111/j.1537-2995.2009.02240.x. Epub 2009 Jun 4.
Transfusion. 2009.
PMID: 19500323
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