1460-2075 < 1460-2083 < 1460-2091

Facettes : Author.f AffPays.f

List of bibliographic references

Number of relevant bibliographic references: 30.
[20-40] [0 - 20][0 - 30]

Ident.	Authors (with country if any)	Title
009320 (2003)	Ramsey A. Saleem ; Sharmila Banerjee-Basu [États-Unis] ; Fred B. Berry [Canada] ; Andreas D. Baxevanis [États-Unis] ; Michael A. Walter [Canada]	Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1
009412 (2003)	Mitsuhiro Kato [Japon] ; William B. Dobyns [États-Unis]	Lissencephaly and the molecular basis of neuronal migration
009449 (2003)	Benjamin M. Kriederman ; Teressa L. Myloyde ; Marlys H. Witte ; Susan L. Dagenais ; Charles L. Witte ; Margaret Rennels ; Michael J. Bernas ; Michelle T. Lynch ; Robert P. Erickson ; Mark S. Caulder ; Naoyuki Miura ; David Jackson [Royaume-Uni] ; Brian P. Brooks [États-Unis] ; Thomas W. Glover	FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome
009931 (2002)	Asma Smahi ; Gilles Courtois ; Smail Hadj Rabia ; Rainer Do Ffinger [France] ; Christine Bodemer ; Arnold Munnich ; Jean-Laurent Casanova [France] ; Alain Israe L	The NF-κB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes
009A20 (2002)	Caroline Thaung [Royaume-Uni] ; Katrine West [Royaume-Uni] ; Brian J. Clark [Royaume-Uni] ; Lisa Mckie [Royaume-Uni] ; Joanne E. Morgan [Royaume-Uni] ; Karen Arnold [Royaume-Uni] ; Patrick M. Nolan [Royaume-Uni] ; Jo Peters [Royaume-Uni] ; A. Jackie Hunter [Royaume-Uni] ; Steve D. M. Brown [Royaume-Uni] ; Ian J. Jackson [Royaume-Uni] ; Sally H. Cross [Royaume-Uni]	Novel ENU-induced eye mutations in the mouse: models for human eye disease
009A37 (2002)	Matthew A. Lines [Canada] ; Kathy Kozlowski [Canada] ; Michael A. Walter [Canada]	Molecular genetics of Axenfeld–Rieger malformations
009B67 (2002)	Douglas B. Gould [États-Unis] ; Simon W. M. John [États-Unis]	Anterior segment dysgenesis and the developmental glaucomas are complex traits
00B967 (1998)	Robert E. Ferrell [États-Unis] ; Kara L. Levinson [États-Unis] ; Judith H. Esman [États-Unis] ; Mark A. Kimak [États-Unis] ; Elizabeth C. Lawrence [États-Unis] ; M. Michael Barmada [États-Unis] ; David N. Finegold [États-Unis]	Hereditary Lymphedema: Evidence for Linkage and Genetic Heterogeneity
00CC76 (1995)	Sandrine Barbaux [France] ; Eric Vilain [France] ; Odile Raoul [France] ; Simone Gilgenkrantz ; Eric Jeandidier ; Denis Chadenas [France] ; Nicole Souleyreau [France] ; Marc Fellous [France] ; Ken Mcelreavey [France]	Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata
00D861 (1993)	Dominique Well [France] ; Marie-France Portnoi ; Jacquellne Levilliers [France] ; Irène Wang [France] ; Michèle Mathieu [France] ; Jean-Louis Talliemite ; Murielle Meler ; Bernard Boudailliez [France] ; Christine Petit [France]	A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata

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