Serveur d'exploration sur le lymphœdème - Exploration (Accueil)

Index « Keywords » - entrée « Heart Defects, Congenital (genetics) »
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Heart Defects, Congenital (etiology) < Heart Defects, Congenital (genetics) < Heart Defects, Congenital (pathology)  Facettes :

List of bibliographic references indexed by Heart Defects, Congenital (genetics)

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000567 (2017) Aisling M. O'Riordan [Irlande (pays)] ; Niamh Mcgrath [Irlande (pays)] ; Farhana Sharif [Irlande (pays)] ; Nuala P. Murphy [Irlande (pays)] ; Orla Franklin [Irlande (pays)] ; Sally Ann Lynch [Irlande (pays)] ; Michael J. O'Grady [Irlande (pays)]Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance.
001C21 (2015) G. Morcaldi ; T. Bellini ; C. Rossi ; M. Maghnie ; F. Boccardo ; E. Bonioli ; C. BelliniLYMPHODYSPLASIA AND KRAS MUTATION: A CASE REPORT AND LITERATURE REVIEW.
00D715 (1991) Giovanni Neri [Italie] ; Marcella Zollino [Italie] ; James F. Reynolds [Italie, États-Unis]The Noonan‐CFC controversy
012A93 (????) Daniela Larizza [Italie] ; Miryam Martinetti ; Jean Michel Dugoujon ; Carmine Tinelli ; Valeria Calcaterra ; Mariaclara Cuccia ; Laura Salvaneschi ; Francesca SeveriParental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome.

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