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

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List of bibliographic references

Number of relevant bibliographic references: 12.
Ident.Authors (with country if any)Title
003471 (2006) Inas Mazen [Égypte] ; Maha S. ZakiUnusual association of simplified gyral pattern and sparse hair in an Egyptian patient with microcephaly-lymphoedema.
003791 (2005) A. Debeer [Belgique] ; E. Steenkiste ; K. Devriendt ; M. MorrenScalp skin lesion in Turner syndrome: more than lymphoedema?
003841 (2005) Pradeep C. Vasudevan [Royaume-Uni] ; Sixto Garcia-Minaur ; Maria Pilar Botella ; Antonio Perez-Aytes ; Nora L. Shannon ; Oliver W J. QuarrellMicrocephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literature.
003A39 (2004) Mariam Patrícia Auada [Brésil] ; Maria Letícia Cintra ; Maria Beatriz Puzzi ; Danilo Viana ; Denise Pontes CavalcantiScalp lesions in Turner syndrome: a result of lymphoedema?
003B30 (2004) Vera Lúcia Gil Da Silva Lopes ; Maria Leine Guion-Almeida ; Silvyo David Araújo GiffoniFrontonasal dysplasia, neuronal migration error and lymphoedema of limbs.
003D81 (2003) L I Al-Gazali ; J. Hertecant ; R. Ahmed ; N A Khan ; R. PadmanabhanFurther delineation of Hennekam syndrome.
004354 (2000) P. Huppke [Allemagne] ; H J Christen ; B. Sattler ; F. HanefeldTwo brothers with Hennekam syndrome and cerebral abnormalities.
004873 (1998) L I Al-Gazali ; D. BakalinovaAutosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance.
004A80 (1996) C. Kozma [États-Unis] ; N. Scribanu ; E. GershThe microcephaly-lymphoedema syndrome: report of an additional family.
004E77 (1994) I K Temple [Royaume-Uni] ; J R CollinDistichiasis-lymphoedema syndrome: a family report.
004F05 (1994) M. Genuardi [Italie] ; F. Calvieri ; C. Tozzi ; R. Coslovi ; G. NeriA new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.
005075 (1993) S R Phaoke [Inde] ; A K Sharma ; S S AgarawalA new syndrome of multiple joint dislocations with metaphyseal dysplasia.

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