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Human Molecular Genetics|June 1, 1993
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndromeM Jeanpierre, C Turleau, A Aurias, et al.Human Genetics|June 1, 1997
alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissuesP Miniou, M Jeanpierre, D Bourc'his, et al.Human Genetics|March 1, 1989
Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probeE Viegas-Péquignot, M Jeanpierre, A M Dutrillaux, et al.Human Genetics|August 1, 1993
No relationship between genetic instability in Bloom's syndrome and DNA hypomethylation of some major repetitive sequencesP Noguiez, C Jaulin, F Praz, et al.Annales De Cardiologie Et D'Angeiologie|May 1, 1993
[Late complication of blunt injuries of the thorax: acute pericarditis. Apropos of a case]B Maillier, L Chapoutot, D Metz, et al.Human Genetics|July 1, 1993
Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell linesA Almeida, N Kokalj-Vokac, D Lefrancois, et al.Neurology|November 18, 1998
Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophyP Laforêt, C de Toma, B Eymard, et al.Plastic and Reconstructive Surgery|January 25, 2023
A Contemporary Review of the Role of Facial Prostheses in Complex Facial ReconstructionAllison A Slijepcevic, Azadeh Afshari, Ann E Vitale, et al.Human Genetics|October 1, 1986
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophyJ Chelly, F Marlhens, B Le Marec, et al.Journal of Medical Genetics|June 1, 1991
Contribution to carrier detection and genetic counselling in X linked retinoschisisJ Kaplan, A Pelet, H Hentati, et al.Pageof 6