P Hilbert

Publications by Year

Research Areas

Genetic Syndromes and Imprinting, Epigenetics and DNA Methylation, Hearing, Cochlea, Tinnitus, Genetics, Pulmonary Hypertension Research and Treatments, Genomic variations and chromosomal abnormalities

Most-Cited Works

• → Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis(1998)216 cited
• Low frequency of the GJB6 342 Kb deletion in the belgian deaf population.(2002)
• Lack of segregation of a Marfan-like phenotype associating marfanoie habitus and mitral valve disease with fibrillin gene on chromosome 15(1994)
• Use of denaturing high performance liquid chromatography (DHPLC) for connexin 26 gene mutation screening.(1999)
• Identification of 15 novel mutations in Sotos syndrome(2011)
• Recherche par génétique positionnelle de gènes impliqués dans des caractères quantitatifs: A. le caractère culard bovin - B. l'hypertension artérielle du rat(1993)