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Serveur d'exploration sur le lymphœdème - Checkpoint (PubMed)

Index « ISSN » - entrée « 1552-4825 »
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1552-454X < 1552-4825 < 1552-4833  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 11.
Ident.Authors (with country if any)Title
003185 (2007) Shoji Yabuki [Japon] ; Shin-Ichi Kikuchi ; Shiro IkegawaSpinal extradural arachnoid cysts associated with distichiasis and lymphedema.
003263 (2007) Karmen M. Trzupek [États-Unis] ; Rena E. Falk ; Joseph L. Demer ; Richard G. WeleberMicrocephaly with chorioretinopathy in a brother-sister pair: evidence for germ line mosaicism and further delineation of the ocular phenotype.
003279 (2007) M A M. Van Steensel [Pays-Bas] ; M. Van Geel ; C. Schrander-Stumpel ; P M Steijlen ; J C J M. VeraartLymphedema, cardiac septal defects, and characteristic facies: possible new case of Irons-Bianchi syndrome.
003420 (2007) Matthew G. Butler [États-Unis] ; Susan L. Dagenais ; Stanley G. Rockson ; Thomas W. GloverA novel VEGFR3 mutation causes Milroy disease.
003631 (2006) Salim Aftimos ; Malcom BattinFamilial congenital non-immune hydrops.
003632 (2006) David A. Stevenson [États-Unis] ; Theodore J. Pysher ; Robert M. Ward ; John C. CareyFamilial congenital non-immune hydrops, chylothorax, and pulmonary lymphangiectasia.
003944 (2005) Eugenio Bonioli [Italie] ; Raoul C. Hennekam ; Gianantonio Spena ; Guido Morcaldi ; Antonio Di Stefano ; Giovanni Serra ; Carlo BelliniAplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia.
003C00 (2004) Cagri Yildirim-Toruner [États-Unis] ; Kavitha Subramanian ; Lamya El Manjra ; Emily Chen ; Stanley Goldstein ; Emilia VitaleA novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus.
003D13 (2003) Brad Angle [États-Unis] ; Frank Yen ; Joseph H. Hersh ; Gordon GowansPatient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.
003D76 (2003) Carlo Bellini [Italie] ; Massimo Mazzella ; Cesare Arioni ; Corradino Campisi ; Gioconda Taddei ; Paolo Tomà ; Francesco Boccardo ; Raoul C. Hennekam ; Giovanni SerraHennekam syndrome presenting as nonimmune hydrops fetalis, congenital chylothorax, and congenital pulmonary lymphangiectasia.
003E47 (2003) Anita Rauch [Allemagne] ; Maike Beese ; Ertan Mayatepek ; Helmut-Günther Dörr ; Dieter Wenzel ; André Reis ; Udo TrautmannA novel 5q35.3 subtelomeric deletion syndrome.

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