Wuchereria bancrofti < X Chromosome < X Chromosome Inactivation

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List of bibliographic references indexed by X Chromosome

Number of relevant bibliographic references: 9.

Ident.	Authors (with country if any)	Title
009943 (2001)	R. Döffinger [France] ; A. Smahi ; C. Bessia ; F. Geissmann ; J. Feinberg ; A. Durandy ; C. Bodemer ; S. Kenwrick ; S. Dupuis-Girod ; S. Blanche ; P. Wood ; S H Rabia ; D J Headon ; P A Overbeek ; F. Le Deist ; S M Holland ; K. Belani ; D S Kumararatne ; A. Fischer ; R. Shapiro ; M E Conley ; E. Reimund ; H. Kalhoff ; M. Abinun ; A. Munnich ; A. Israël ; G. Courtois ; J L Casanova	X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.
009976 (2001)	K A Leppig [États-Unis] ; C M Disteche	Ring X and other structural X chromosome abnormalities: X inactivation and phenotype.
009E36 (2001)	Marika J. Karkkainen [Finlande] ; Lotta Jussila [Finlande] ; Kari Alitalo [Finlande] ; Robert E. Ferrell ; David N. Finegold	Molecular regulation of lymphangiogenesis and targets for tissue oedema
009E93 (2001)	S. Mansour [Royaume-Uni] ; H. Woffendin [Royaume-Uni] ; S. Mitton [Royaume-Uni] ; I. Jeffery [Royaume-Uni] ; T. Jakins [Royaume-Uni] ; S. Kenwrick [Royaume-Uni] ; V. A. Murday [Royaume-Uni]	Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection
00A031 (2001)	Catherine A. Boucher ; Carole A. Sargent ; Tsutomu Ogata ; Nabeel A. Affara	Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location [Original article] [Original article]
00AA12 (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.
00AD75 (1999)	A. Tsezou ; Ch Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; Em Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani [Chypre (pays)] ; Ch Theodoridis ; Pc Patsalis [Chypre (pays)] ; N. Moschonas ; S. Kitsiou	Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy
00B524 (1998)	Andrew R. Zinn [États-Unis] ; Vijay S. Tonk ; Zhong Chen ; Wendy L. Flejter ; H. Allen Gardner ; Rudy Guerra ; Harvey Kushner [États-Unis] ; Stuart Schwartz ; Virginia P. Sybert ; Daniel L. Van Dyke ; Judith L. Ross [États-Unis]	Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1
00F527 (1983)	Claude S. Dahlberg [États-Unis] ; Claude S. Borer [États-Unis] ; Kermit L. Newcomer [États-Unis] ; Wilfrido R. Yutuc [États-Unis]	Autosomal or X‐linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy

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