Congenital imprinting disorders: Eucid.net -a network to decipher their aetiology and to improve the diagnostic and clinical care

Clinical Epigenetics

Volumn 7, Issue 1, 2015, Pages

  Eggermann, Thomas ^a,l   Netchine, Irène ^b,c   Temple, Karen ^d   Tümer, Zeynep ^e   Monk, David ^f   Mackay, Deborah ^d   Grønskov, Karin ^e   Riccio, Andrea ^g,h   Linglart, Agnès ^i,j   Maher, Eamonn R ^k  

^a RWTH AACHEN UNIVERSITY   (Germany)

^b CENTRE DE RECHERCHE SAINT ANTOINE   (France)

^c ARMAND TROUSSEAU HOSPITAL   (France)

^d PRINCESS ANNE HOSPITAL   (United Kingdom)

^e Rigshospitalet   (Denmark)

^f HOSPITAL DURAN I REYNALS   (Spain)

^g SECOND UNIVERSITY OF NAPLES   (Italy)

^h INSTITUTE OF GENETICS AND BIOPHYSICS ADRIANO BUZZATI TRAVERSO   (Italy)

ⁱ ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^j INSERM   (France)

^k UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^l UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

more..

Author keywords

Epimutation; EUCID.net; Imprinted genes; Imprinting disorders; Networking; Uniparental disomy

Indexed keywords

ARTICLE; BECKWITH WIEDEMANN SYNDROME; CAPACITY BUILDING; CONGENITAL DISORDER; GENE DELETION; GENE MUTATION; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; IMPRINTING DISORDER; INFORMATION DISSEMINATION; KAGAMI OGATA SYNDROME; MOLECULAR BIOLOGY; MOLECULAR DIAGNOSTICS; MOLECULAR GENETICS; MOLECULAR IMPRINTING; NEWBORN DIABETES MELLITUS; ORGANIZATION; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PSEUDOHYPOPARATHYROIDISM; SILVER RUSSELL SYNDROME; TEMPLE SYNDROME; TRANSIENT NEONATAL DIABETES MELLITUS; UNIPARENTAL DISOMY;

EID: 84927138888     PISSN: 18687075     EISSN: 18687083     Source Type: Journal    
DOI: 10.1186/s13148-015-0050-z     Document Type: Article

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