Phenobarbital (therapeutic use) < Phenotype < Phenprocoumon (administration & dosage)

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List of bibliographic references

Number of relevant bibliographic references: 117.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000081 (1999)	D. Mowat [Australie] ; A. Jauch ; L. Robson ; A. Smith	Duplication within chromosome 5q characterized by fluorescence in situ hybridization.
000099 (1999)	M A Kron [États-Unis] ; B. Ramirez ; V. Belizario ; J P Pandey	Immunoglobulin allotypes among the Bicolanos of Sorsogon province, Luzon, Philippines: implications of phenotypes for filariasis.
000164 (1999)	S. Babu [États-Unis] ; L D Shultz ; T V Rajan	T cells facilitate Brugia malayi development in TCRalpha(null) mice.
000221 (1999)	F. Haverkamp [Allemagne] ; J. Wölfle ; K. Zerres ; O. Butenandt ; P. Amendt ; B P Hauffa ; E. Weimann ; M. Bettendorf ; E. Keller ; R. Mühlenberg ; C J Partsch ; W G Sippell ; C. Hoppe	Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure.
000260 (1999)	A. Tsezou [Grèce] ; C. Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; E. Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani ; C. Theodoridis ; P C Patsalis ; N. Moschonas ; S. Kitsiou	Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.
000428 (2000)	S E Hong [États-Unis] ; Y Y Shugart ; D T Huang ; S A Shahwan ; P E Grant ; J O Hourihane ; N D Martin ; C A Walsh	Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
000531 (2001)	T. M Kinen [Finlande] ; L. Jussila ; T. Veikkola ; T. Karpanen ; M I Kettunen ; K J Pulkkanen ; R. Kauppinen ; D G Jackson ; H. Kubo ; S. Nishikawa ; S. Yl Herttuala ; Kari Alitalo [Finlande]	Inhibition of lymphangiogenesis with resulting lymphedema in transgenic mice expressing soluble VEGF receptor-3.
000535 (2000)	R. Bell ; G. Brice ; A. Child ; V. Murday ; S. Mansour ; C. Sandy ; J. Collin ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; D. Callen ; K. Burnand ; S. Jeffery	Reduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb
000599 (2001)	L R Osborne	'Forkhead' gene expression balanced on a knife-edge.
000714 (2001)	K A Leppig [États-Unis] ; C M Disteche	Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
000754 (2001)	C. Boucher ; C. Sargent ; T. Ogata ; N. Affara	Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location
000799 (2001)	R. Erickson ; S. Dagenais ; M. Caulder ; C. Downs ; G. Herman ; M. Jones ; W. Kerstjens-Frederi. ; A. Lidral ; M. Mcdonald ; C. Nelson ; M. Witte ; T. Glover	Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations
000A31 (2002)	G. Brice ; S. Mansour ; R. Bell ; J. Collin ; A. Child ; A. Brady ; M. Sarfarazi ; K. Burnand ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; V. Murday	Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
000B81 (2002)	M. Bahuau [France] ; C. Houdayer ; M. Tredano ; V. Soupre ; R. Couderc ; M-P Vazquez	FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate.
000B96 (2003)	Brad Angle [États-Unis] ; Frank Yen ; Joseph H. Hersh ; Gordon Gowans	Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome.
000D50 (2003)	Alexandre Irrthum [Belgique] ; Koenraad Devriendt [Belgique] ; David Chitayat [Canada] ; Gert Matthijs [Belgique] ; Conrad Glade [Pays-Bas] ; Peter M. Steijlen [Pays-Bas] ; Jean-Pierre Fryns [Belgique] ; Maurice A. Van Steensel [Pays-Bas] ; Miikka Vikkula [Belgique]	Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia
000E31 (2003)	Anita Rauch [Allemagne] ; Maike Beese ; Ertan Mayatepek ; Helmut-Günther Dörr ; Dieter Wenzel ; André Reis ; Udo Trautmann	A novel 5q35.3 subtelomeric deletion syndrome.
001A27 (2004)	Mariam Patrícia Auada [Brésil] ; Maria Letícia Cintra ; Maria Beatriz Puzzi ; Danilo Viana ; Denise Pontes Cavalcanti	Scalp lesions in Turner syndrome: a result of lymphoedema?
001C67 (2003)	Michael S. Pepper [Suisse]	Literature watch. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
001C97 (2005)	G. Brice ; A. Child ; A. Evans ; R. Bell ; S. Mansour ; K. Burnand ; M. Sarfarazi ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]	Milroy disease and the VEGFR-3 mutation phenotype
001D24 (2005)	Subash Babu [États-Unis] ; Carla P. Blauvelt ; V. Kumaraswami ; Thomas B. Nutman	Chemokine receptors of T cells and of B cells in lymphatic filarial infection: a role for CCR9 in pathogenesis.

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